CN100467436C - Process for preparing alkoxy- and aryloxy-phenols - Google Patents
Process for preparing alkoxy- and aryloxy-phenols Download PDFInfo
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- CN100467436C CN100467436C CN 200480010413 CN200480010413A CN100467436C CN 100467436 C CN100467436 C CN 100467436C CN 200480010413 CN200480010413 CN 200480010413 CN 200480010413 A CN200480010413 A CN 200480010413A CN 100467436 C CN100467436 C CN 100467436C
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- phenol
- acid
- ketone
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- 238000004519 manufacturing process Methods 0.000 title abstract description 3
- 150000002576 ketones Chemical class 0.000 claims abstract description 35
- 150000002148 esters Chemical class 0.000 claims abstract description 29
- 150000004965 peroxy acids Chemical class 0.000 claims abstract description 11
- 230000001590 oxidative effect Effects 0.000 claims abstract description 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 94
- 238000000034 method Methods 0.000 claims description 56
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 45
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 38
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 31
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 31
- 238000006243 chemical reaction Methods 0.000 claims description 26
- 239000012074 organic phase Substances 0.000 claims description 26
- 239000000203 mixture Substances 0.000 claims description 24
- -1 aryloxy phenol Chemical compound 0.000 claims description 22
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical group [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 claims description 20
- 125000003545 alkoxy group Chemical group 0.000 claims description 19
- 239000011541 reaction mixture Substances 0.000 claims description 17
- 235000019253 formic acid Nutrition 0.000 claims description 16
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- 238000002425 crystallisation Methods 0.000 claims description 14
- 230000008025 crystallization Effects 0.000 claims description 14
- 238000006460 hydrolysis reaction Methods 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 10
- 230000007062 hydrolysis Effects 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 9
- 239000008346 aqueous phase Substances 0.000 claims description 8
- 238000005903 acid hydrolysis reaction Methods 0.000 claims description 7
- 238000000605 extraction Methods 0.000 claims description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 6
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 claims description 6
- 238000005904 alkaline hydrolysis reaction Methods 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 239000012442 inert solvent Substances 0.000 claims description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 6
- 239000003444 phase transfer catalyst Substances 0.000 claims description 6
- 238000004821 distillation Methods 0.000 claims description 5
- 238000001704 evaporation Methods 0.000 claims description 5
- 150000007522 mineralic acids Chemical class 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical group CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 4
- SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 claims description 4
- 230000008020 evaporation Effects 0.000 claims description 4
- 150000007524 organic acids Chemical class 0.000 claims description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 4
- 159000000000 sodium salts Chemical class 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 3
- XCRBXWCUXJNEFX-UHFFFAOYSA-N peroxybenzoic acid Chemical compound OOC(=O)C1=CC=CC=C1 XCRBXWCUXJNEFX-UHFFFAOYSA-N 0.000 claims description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 2
- 230000001476 alcoholic effect Effects 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- 238000005815 base catalysis Methods 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
- 238000004090 dissolution Methods 0.000 claims description 2
- 238000010931 ester hydrolysis Methods 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 2
- 230000009467 reduction Effects 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 238000009834 vaporization Methods 0.000 claims description 2
- 230000008016 vaporization Effects 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 150000004967 organic peroxy acids Chemical class 0.000 claims 1
- 239000000047 product Substances 0.000 description 22
- LUSZGTFNYDARNI-UHFFFAOYSA-N Sesamol Natural products OC1=CC=C2OCOC2=C1 LUSZGTFNYDARNI-UHFFFAOYSA-N 0.000 description 15
- UIOFUWFRIANQPC-JKIFEVAISA-N Floxacillin Chemical compound N([C@@H]1C(N2[C@H](C(C)(C)S[C@@H]21)C(O)=O)=O)C(=O)C1=C(C)ON=C1C1=C(F)C=CC=C1Cl UIOFUWFRIANQPC-JKIFEVAISA-N 0.000 description 14
- 235000011121 sodium hydroxide Nutrition 0.000 description 14
- 229940083608 sodium hydroxide Drugs 0.000 description 12
- 230000036571 hydration Effects 0.000 description 11
- 238000006703 hydration reaction Methods 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Substances CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 9
- 238000007254 oxidation reaction Methods 0.000 description 9
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 8
- 241000207961 Sesamum Species 0.000 description 8
- 235000003434 Sesamum indicum Nutrition 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 239000012071 phase Substances 0.000 description 7
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- 239000000376 reactant Substances 0.000 description 5
- 239000003643 water by type Substances 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 150000001299 aldehydes Chemical class 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 150000003934 aromatic aldehydes Chemical class 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 230000003301 hydrolyzing effect Effects 0.000 description 3
- 235000019260 propionic acid Nutrition 0.000 description 3
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
- FTNJQNQLEGKTGD-UHFFFAOYSA-N 1,3-benzodioxole Chemical compound C1=CC=C2OCOC2=C1 FTNJQNQLEGKTGD-UHFFFAOYSA-N 0.000 description 2
- 238000006220 Baeyer-Villiger oxidation reaction Methods 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000008365 aromatic ketones Chemical class 0.000 description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
- 239000012965 benzophenone Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
- HGUFODBRKLSHSI-UHFFFAOYSA-N 2,3,7,8-tetrachloro-dibenzo-p-dioxin Chemical compound O1C2=CC(Cl)=C(Cl)C=C2OC2=C1C=C(Cl)C(Cl)=C2 HGUFODBRKLSHSI-UHFFFAOYSA-N 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical class CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 description 1
- 238000007171 acid catalysis Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical class O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- LULAYUGMBFYYEX-UHFFFAOYSA-N metachloroperbenzoic acid Natural products OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000005544 phthalimido group Chemical group 0.000 description 1
- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229940065287 selenium compound Drugs 0.000 description 1
- 150000003343 selenium compounds Chemical class 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to atoms of the carbocyclic ring
- C07D317/64—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
- C07C41/26—Preparation of ethers by reactions not forming ether-oxygen bonds by introduction of hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/39—Preparation of carboxylic acid esters by oxidation of groups which are precursors for the acid moiety of the ester
- C07C67/42—Preparation of carboxylic acid esters by oxidation of groups which are precursors for the acid moiety of the ester by oxidation of secondary alcohols or ketones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/10—1,4-Dioxanes; Hydrogenated 1,4-dioxanes
- C07D319/14—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
- C07D319/16—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D319/18—Ethylenedioxybenzenes, not substituted on the hetero ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The present invention provides a process for preparing alkoxy- and aryloxy-phenols, comprising oxidizing the ketone of formula (I) with peracids to give the corresponding ester of formula (II) which is then hydrolysed to give the corresponding aryloxy- or alkoxy-phenol.
Description
Technical field
The present invention relates to a kind of method for preparing alkoxyl group phenol and aryloxy phenol.
Background technology
Alkoxyl group phenol and aryloxy phenol are the products with extensive industrial use.Wherein, for example, sesamol, just 3,4-(methylene-dioxy) phenol is a kind ofly to be used as intermediate and can be used as antioxidant, antiseptic-germicide and weedicide and to be used for the compound of cosmetic industry in the preparation of medicament production.
In synthetic method, a kind of very frequent reaction of using is Baeyer-Villiger reaction, and it has used corresponding aromatic aldehyde.This reaction comprises aldehyde cpd is changed into corresponding phenol manthanoate and produces phenolic compound with posthydrolysis.
For example at US 5,840, in 997, described and used the alkoxyl group phenol of corresponding aldehyde and the preparation of aryloxy phenol.Use methylene dichloride to make solvent, in heterogeneous, carry out this oxidising process with hydrogen peroxide and formic acid.
Patent application EP 1167365 A1 have described a kind of by use the method for the corresponding piperonylaldehyde of peracetic acid oxidation with synthetic sesamol in the presence of formic acid in organic solvent.
At Ind.J.Chem.1983, in 22,1150, in the chlorinated solvent of methylene dichloride and so on, use metachloroperbenzoic acid with the aromatic aldehyde compound oxidation to obtain phenol derivatives.
At SU688, in 492, in the chlorinated solvent of methylene dichloride and so on, use the performic oxidation aldehydes.
Aromatic ketone is oxidized to corresponding phenol almost only is used for methyl phenyl ketone and benzophenone, and, therefore do not consider C owing to obtain the mixture of lower reaction of selectivity and generation ester class usually
2-C
6The higher homologue of aliphatic ketone (referring to March, Advanced Organic Chemistry, 5
ThEdition, Wiley, p.1417).
J.Am.Chem.Soc.
71, 14 (1949) have described with extremely long reaction times (10 days) some ketone of usefulness peroxybenzoic acid oxidation in chloroform.
Synthesis, 1989,167-171 has described with high density (90%) hydrogen peroxide and under the condition that selenium compound exists as oxide catalyst methyl phenyl ketone has been oxidized to phenol.
Synthesis Comm.29 (21), 3781-3791 (1999) have described with hydrogen peroxide oxidation aromatic aldehyde, methyl phenyl ketone and benzophenone, and this is reflected at the vitriolic existence and activates with boric acid down.
Do not mention the aromatic ketone that is different from methyl phenyl ketone or benzophenone derivative about use.
Because the high density of hydrogen peroxide, to the existence and the very long reaction times of the oxide catalyst of the serious boron of environmental influence or selenium and so on, described condition almost can't be used.
Therefore, impel the technician of alkoxyl group phenol and aryloxy phenol preparation field to consider the bigger advantage of the corresponding aromatic aldehyde of oxidation.
Brief summary of the invention
The applicant is surprised to find that, can overcome the defective of prior art by method of the present invention, and method of the present invention is included in the ketone of use formula (I) in the oxidizing reaction of using peracid
X wherein
1, X
2, m, n and R be as described in hereinafter, this peracid is preparation or on-site preparation by hydrogen peroxide in inert solvent and corresponding organic acid effect and in advance.
Use ketone can realize non-anhydrous response environment, reason is that corresponding ester does not have activity so to acidic hydrolysis, this during with manthanoate that the oxidation of using by aldehyde cpd produces situation different, can make thus and reduce to minimum because of the by product of oxidation generation.
Detailed Description Of The Invention
The present invention relates to make alkoxyl group phenol and aryloxy phenol, wherein X by the ketone of formula (I)
1And X
2, identical or different, be straight or branched C
1-C
8Alkyl is preferably C
1-C
4Alkyl, unsubstituted or by C
1-C
8Alkyl, by trifluoromethyl or the C that replaced by the halogen of for example chlorine, bromine, iodine and fluorine
6-C
10Aryl, or (OX
1)
n(OX
2) m is equivalent to group O-T-O together, T is CH herein
2, CH
2CH
2Or C (Me)
2And be preferably CH
2Do not replace or by C
1-C
2The C that alkyl replaces
6Be preferred.N and m are 0,1 or 2, and its condition is for they are not 0 all the time when n=m; R is straight or branched C
2-C
6Alkyl or cyclohexyl are preferably C
2-C
3Alkyl, more preferably ethyl.
The present invention includes the method for the compound conversion of formula (I), wherein X
1, X
2, n, m and R have aforementioned implication, it comprises the following steps:
A) in inert organic solvents with the compound of peracid oxidation-type (I) to prepare the ester of corresponding formula (II);
X wherein
1, X
2, n, m and R have aforementioned implication;
B) the ester hydrolysis of formula (II) is to prepare the phenol of corresponding formula (III)
X wherein
1, X
2, n, m and R have aforementioned implication.
As previously mentioned, by Baeyer-Villiger reaction, the oxidation of ketones that uses the peracid of previously prepared or on-the-spot generation will be dissolved in the formula (I) in the inert solvent is corresponding ester, wherein peracid preference such as peroxyformic acid, peracetic acid, cross toxilic acid, peroxybenzoic acid and cross phthalic acid.The peroxyformic acid of the reaction on-site preparation by formic acid and hydrogen peroxide most preferably.The amount of formic acid is that every mole of ketone 1.5 to 8 equivalents do not wait, and is preferably every mole of ketone 2 to 5 equivalents and does not wait.Every mole of ketone uses 1 to 6 normal hydrogen peroxide, and preferred every mole of ketone uses 1.2 to 3 normal hydrogen peroxide.
This inert solvent is a kind of and water unmixing, and the ketone that can dissolution type (I) and the organic solvent of carboxylic acid or corresponding peracid.
This inert solvent is selected from pentane, hexane, heptane, octane and their mixture, methylene dichloride, chloroform, tetracol phenixin and ethylene dichloride.The chlorating solvent is preferred.Methylene dichloride is particularly preferred.
The solvent volume of the ketone correspondence of the formula of using in every mole of step (a) (I) is 0.05 to rise to 1.5 liters, and preferred 0.05 rises to 1 liter, more preferably 0.2 rises to 0.5 liter.
Used hydrogen peroxide is commercially available and is easy to use, its concentration by weight/volumeter do not wait between 30% to 35%.
The concentration of used formic acid by weight/the weight meter is greater than 80%, be preferably greater than or equal 85%.
Between 20 ℃ and 80 ℃, preferably between 30 ℃ to 50 ℃, more preferably under the temperature between 40 ℃ to 50 ℃, carry out oxidizing reaction.
Under alkalescence or sour environment, carry out the hydrolysis of the ester of formula (II).
Alkaline environment is preferred.
When being hydrolyzed reaction under alkaline environment, the alkali of adding is the alkaline hydrated oxide of aqueous solution form.Sodium hydroxide is preferred.
Amount with every mole of ester 3 to 6 Equivalent Hydrogen sodium oxides adds alkali.
The sodium hydroxide of every mole of ester 4 molar equivalents is preferred.
Reaction solvent is a used identical inert solvent in the reaction with step (a).
In the case, after removing water, use the identical reaction mixture that generates by step (a).
According to particularly preferred embodiment, under having the situation of phase-transfer catalyst, carry out the hydrolysis reaction in the alkaline environment, more preferably use tetrabutylammonium chloride or Aliquat 360.
Preferably the mol ratio with the ester 1/20 to 1/90 of every mole of formula (II) adds phase-transfer catalyst.The mol ratio of every mole of ester 1/40 to 1/80 is especially preferred.
According to prior art, at C
1-C
10In the alcoholic solvent, preferably at C
1-C
3In the alcohol, more preferably in methyl alcohol, carry out acid hydrolytic reaction.
Acid as catalyzer is generally strong inorganic acid, is preferably the vitriol oil of 96% (%w/w).
In the case, the mol ratio with 1% to 2% mole of the ester of every mole of formula (II) adds acid.
Between 30 ℃ to 60 ℃, more preferably under 40 ℃, carry out acid hydrolytic reaction.
Preferably carry out from the alkoxyl group phenol of the formula (III) of acid hydrolytic reaction (this reaction according to aforementioned preferred operations condition, especially carry out) or the separation of aryloxy phenol with sulfuric acid according to the method that comprises the following steps:
A) reduction vaporization methyl alcohol;
B) dissolve residuum once more with methylene dichloride, and add sodium hydroxide solution (being preferably 2M); Removal contains the organic phase of ketone and unreacted ester;
C) use organic or inorganic acid, preferred 37% HCl, the aqueous phase as acidified of sodium salt of phenol that will contain formula (III) is with the alkoxyl group phenol or the aryloxy phenol of release type (III), and it uses dichloromethane extraction;
D) with methylene dichloride evaporation to obtain residue, then with its distillation and/or crystallization to make alkoxyl group phenol or aryloxy phenol.
The alkoxyl group phenol or the aryloxy phenol reaction mixture of the formula (III) that alkaline hydrolysis is generated separate, and it carries out in step (b) by the method that comprises following operation steps:
A ') two with reaction mixture are separated; Removal contains the organic phase of unreacted ketone, unhydrolysed ester and (if possible) catalyzer, simultaneously to handle water with aforementioned (C) of the product that is used for generating and identical method (D) by acid hydrolysis, but change in the case, step (B ') and (C ') of such definition into;
B ') use strong inorganic acid, be preferably 37% HCl, the aqueous phase as acidified of sodium salt that will contain the alkoxyl group phenol of formula (III) or aryloxy phenol is to discharge the corresponding phenolic derivative, and it uses dichloromethane extraction.
C ') the evaporation methylene dichloride is up to obtaining residue, then with residue distillation and/or alkoxyl group phenol and the aryloxy amphyl of crystallization to make formula (III).
The all recirculation in step (a) easily of unreacted ketone that obtains by the hydrolysis under acid catalysis and the base catalysis.
In this regard, if reaction mixture derives from acidic hydrolysis, then with the organic phase recirculation of step (a), and if in alkaline environment, be hydrolyzed, then the organic phase with step (A ') is used for recirculation.
In the case, organic phase not only contains the ester of ketone and non-hydrolysis, also contains phase-transfer catalyst.
The applicant surprisingly finds, contains the organic phase of described phase-transfer catalyst by recirculation, can improve transformation efficiency, selectivity and the reaction yield of required ester, and need not further to add catalyzer in hydrolysis circulation subsequently.
Provide the ketone that especially is preferably used as initial reactant below and can adopt the inventive method by its corresponding phenol that makes.
R wherein
1Be ethyl or n-propyl.
Aforementioned ketone maybe can be buied according to prior art for preparing.R is that ethyl and O-T-O are CH in the ketone of formula (I)
2The time, the latter such as US 6,342,613 described being prepared.
Be illustrative and the preparation embodiment of nonrestrictive employing the inventive method below.
Embodiment 1
Synthetic (ester (II), R=ethyl, m=1, the X of propionic acid sesame ester
1And X
2Be equivalent to group O-T-O, T is CH herein together
2).
With 460 gram (2.5 moles) 1,3-benzo dioxolane (benzodioxol)-5-third-1-ketone (ketone of formula (1), R=ethyl wherein, m=1, X
1And X
2Be equivalent to the O-T-O group, T is CH herein together
2) (purity 96.7%), 650 milliliters of methylene dichloride and 249.6 gram (5.3 moles) formic acid (98%) add in the flasks, and with the speed of 0.35 gram/minute with dripping 339.2 hydrogen peroxide that restrain (3.5 moles) 35% in 6 hours.Reaction is separated when finishing.With 130 milliliters of dichloromethane extraction waters; Na with 140 grams 10%
2SO
3Wash organic phase to eliminate superoxide with 130 ml waters.To be separated, and under vacuum, under 30 ℃/23 millibars, organic phase is evaporated; With respect to the yield that transforms ketone is 94%.
Embodiment 2AThe acidic hydrolysis of-propionic acid sesame ester
The sulfuric acid of 1200 ml methanol and 3.4 grams 96% is added in the crude reaction product of embodiment 1.Mixture was stirred 9 hours down at 40 ℃, cooling then, and under vacuum, under 30 ℃/23 millibars with solvent evaporation.
Residue is dissolved in again in 500 milliliters the methylene dichloride, and to the sodium hydroxide that wherein adds 790 milliliters of 2M.
Then mixture was stirred 10 minutes, separate each phase.With 50 milliliters of dichloromethane extraction waters.The organic phase that contains ketone and unhydrolysed ester as recirculation as described in the following examples 3A.
Adding 37%HCI to the aqueous phase that contains sesame acid sodium then, is 8.5 up to pH, to make the sesamol of unbound state, then with its dichloromethane extraction with 50 milliliters.Under vacuum, under 30 ℃/23 millibars, concentrate the organic phase that contains sesamol.
Under 116 ℃/3-4 millibar, distill sesamol; Hydrolysis yield: 94.3%.
Embodiment 2BThe alkaline hydrolysis of-propionic acid sesame ester
The sodium hydroxide of 1325 milliliters of 4M and the hydration tetrabutylammonium chloride of 3.6 gram (13 mmoles) 98% are added in the organic phase in methylene dichloride of the last acquisition of reaction among the embodiment 1.After at room temperature stirring 8 hours, separate each phase.200 milliliters of methylene dichloride are added aqueous phases, and to add 37% HCl be 8.5 up to pH, to discharge sesamol, sesamol enters organic phase.Separate organic phase, and under vacuum, under 30 ℃/23 millibars evaporating solvent.Under 116 ℃/23 millibars, distill sesamol; Hydrolysis yield: 95.8%.
Embodiment 3AThe recirculation of-the product that generates by acidic hydrolysis
Be set forth in as embodiment 2A in the sour environment after the hydrolysis, and in methylene dichloride, handle so that make sesamol enter water with the form of sesame acid sodium with aqueous sodium hydroxide solution then, make the ketone and the reaction of unhydrolysed ester that are dissolved in the organic phase as described in example 1 above.
With with embodiment 1 in identical amount add ketone, adopt the identical reaction conditions that provides among the embodiment 1 and the reactant of same amount.Make propionic acid sesame ester with 85% yield with respect to converted product.
Embodiment 3BThe recirculation of-the product that generates by alkaline hydrolysis
Be set forth in as embodiment 2B in the alkaline environment after the hydrolysis, the organic solution that will contain unreacted ketone and unhydrolysed ester complements to the same amount of ketone described in the embodiment 1, and reaction as in Example 1.By with embodiment 3B in the identical operations method, and adopt the reaction that is hydrolyzed of identical propionic acid sesame ester/NaOH mol ratio, no longer further add catalyzer.
The distillation back makes sesamol with 94% hydrolysis yield.
Embodiment 4Synthesizing of-propionic acid sesame ester
With 233.2 grams 1,3-benzo dioxolane (benzodioxol)-5-third-1-ketone (1.25 moles) (purity 96.4%) and 325 milliliters of CH
2Cl
2Mix in the reactor that adds 2 liters.
The HCOOH that adds 142.1 gram (2.62 moles) 85% then.Temperature is increased to 47 ℃, adds the H of 170.0 gram (1.75 moles) 35% with 6 hours (with the speed of 0.47 gram/minute)
2O
2
Under refluxing, keep after 6 hours, in last each phase of separating of reaction.With 70 gram 10%Na
2SO
3With 60 ml waters washing organic phase.Analyze organic phase by GC, obtain equaling 94.5% with respect to the yield of converted product.
Embodiment 4A-alkaline hydrolysis
2.32 gram (8 mmole) hydration tetrabutylammonium chloride adds in the aforementioned organic phase, and temperature is being remained in 20-25 ℃, with the NaOH that added 664 gram (2.7 moles) 4M in 45 minutes.
After at room temperature stirring 8 hours, separate each phase.
With 100 milliliters of CH
2Cl
2Joining aqueous phase, is 8.5 to the HCl that wherein adds 37% up to pH.Separate each phase.Under vacuum, under 30 ℃/23 millibars, concentrate the organic phase that contains sesamol.
Under 116 ℃/3-4 millibar, distill sesamol, make 82 gram products.
Yield with respect to converted product: 92.3%.
The distilled sesamol of crystallization in 1/2 (v/v) of toluene/hexanaphthene mixture.
The solid that obtains is leached, dry under 40 ℃/23 millibars under vacuum.Making 79 gram concentration is the crystallization sesamol of 99.7%w/w.
Embodiment 5-3,4-dimethoxy phenol synthetic
With the mixture heating up to 40 of the formic acid of 9.6 gram (50 mmole) 1-(3,4-dimethoxy-phenyl)-1-acetone, 13 milliliters of methylene dichloride and 5.2 gram (110 mmoles) 95% ℃; The hydrogen peroxide that slowly adds 6.9 gram (70 mmoles) 35% then.
In case hydrogen peroxide adds fully, just mixture was placed 6 hours under refluxing.Then with reaction mixture cooling, organic phase separated and wash, and wash with water at last with the sodium sulfite aqueous solution of 5 milliliter 10% (%w/w).
Hydration tetrabutylammonium chloride with 0.12 gram (0.4 mmole) 98% adds in the organic solution then.At room temperature, under agitation the sodium hydroxide of 32 milliliters of 4M is added in the mixture.
Reaction mixture was heated 6 hours under refluxing, and cooling then is up to being separated into two distinct phases.20 milliliters of methylene dichloride are added aqueous phases, and adding 37% HCI then is about 1 up to the pH value.Organic phase washes, uses dried over sodium sulfate, filtration and evaporation under 30 ℃/24 millibars with water.
Obtain a kind of oil (4.1 gram), use alcohol crystal then, make fusing point thus and be 78-80 ℃ product, its NMR and MS analyze the feature that meets aforesaid compound.
Embodiment 6Synthesizing of-1-4-(phenoxy group) phenol
Be similar to described in the embodiment 5, make the mixtures and 6.0 of the formic acid of 8.7 gram (38 mmole) 1-(4-Phenoxyphenyl)-1-acetone, 13 milliliters of methylene dichloride and 4.5 gram (90 mmoles) 95% restrain the hydroperoxidation of (60 mmoles) 35%.
After handling organic solution as described in example 5 above, in the hydration tetrabutylammonium chloride adding reaction mixture with 0.09 gram (0.32 mmole) 98%, use the sodium-hydroxide treatment of 24 milliliters of 4M then.
After the processing described in the similar embodiment 5, obtain 4.1 gram products, its fusing point after crystallization from sherwood oil is 83-84 ℃, its NMR and MS meet the feature of required compound.
Embodiment 7-3,4-methylene-dioxy phenol synthetic
Be similar to described in the embodiment 5, make 10.0 gram (51 mmole) 1-(1,3-benzo dioxolane (benzodioxol)-5-yl)-1-butanone, 15 milliliters of methylene dichloride, 5.25 mixtures and 7.0 that restrain the formic acid of (108 mmoles) 95% restrain the hydroperoxidation of (72 mmoles) 35%.
After handling organic solution as described in example 5 above, in the hydration tetrabutylammonium chloride adding reaction mixture with 0.109 gram (0.38 mmole) 98%, use the sodium-hydroxide treatment of 31 milliliters of 4M then.
After handling described in the similar embodiment 5, obtain 3.8 gram products, its fusing point after crystallization from hexanaphthene/dichloromethane mixture is 63-65 ℃, its NMR and MS meet the feature of required compound.
Embodiment 8-6-hydroxyl-2,3-dihydro-1,4-Ben Bing dioxine synthetic
Be similar to described in the embodiment 5, make 9.42 gram (49 mmole) 1-(2,3-dihydro-1,4-Ben Bing dioxine-6-yl)-mixtures and 6.8 of the formic acid of 1-acetone, 14 milliliters of methylene dichloride, 5.0 gram (100 mmoles) 95% restrain the hydroperoxidation of (70 mmoles) 35%.
After handling organic solution as described in example 5 above, in the hydration tetrabutylammonium chloride adding reaction mixture with 0.09 gram (0.32 mmole) 98%, and the reaction mixture of such acquisition and the sodium hydroxide of 24 milliliters of 4M are reacted.
After the processing described in the similar embodiment 5, obtain the oily product, it distills under 153-156 ℃/9 millibars, and its NMR and MS meet the feature of required compound.
Embodiment 9Synthesizing of-4-methoxyl group phenol
Be similar to described in the embodiment 5, make 10.0 gram (60 mmole) 1-(4-p-methoxy-phenyl)-1-acetone, 15 milliliters of methylene dichloride, 6.1 mixtures and 8.25 that restrain the formic acid of (130 mmoles) 95% restrain the hydroperoxidation of (85 mmoles) 35%.
After handling organic solution as described in example 5 above, the hydration tetrabutylammonium chloride of 0.16 gram (0.6 mmole) 98% is added in the reaction mixture, and the mixture that makes like this and the sodium hydroxide of 46 milliliters of 4M are reacted.After the processing described in the similar embodiment 5, obtain 5.3 gram products, it is after crystallization from sherwood oil, and fusing point is 54-56 ℃, and its NMR and MS meet the feature of required compound.
Embodiment 10-3,4,5-trimethoxy phenol synthetic
Be similar to described in the embodiment 5, make 11.3 gram (50 mmole) 1-(3,4,5-trimethoxyphenyl)-mixtures and 7.35 of the formic acid of 1-acetone, 15 milliliters of methylene dichloride, 5.5 gram (110 mmoles) 95% restrain the hydroperoxidation of (75 mmoles) 35%.
After handling organic solution as described in example 5 above, 0.12 gram (0.4 mmole) hydration tetrabutylammonium chloride is added in the organic solvent, and the mixture that makes like this and the sodium hydroxide of 32 milliliters of 4M are reacted.
After the processing described in the similar embodiment 5, obtain 1.5 gram products, its fusing point after crystallization from toluene is 146-148 ℃, its NMR and MS meet the feature of required compound.
Embodiment 11-3,4-methylene-dioxy phenol synthetic
With 17.7 gram (100 mmole) 1-(1,3-benzo dioxolane (benzodioxol)-5-yl)-and the mixture heating up to 40 of the diacetyl oxides of 1-acetone, 26 milliliters of methylene dichloride, 22.5 gram (220 mmoles) 98% and single hydration tosic acid of 0.42 gram (2 mmole) ℃, slowly add 14 gram (140 mmole) hydrogen peroxide then.
In case hydrogen peroxide adds and to finish, just with mixture heating up to reflux temperature, subsequently with its cooling, separate each phase.
Handle waters with 50 milliliters of methylene dichloride, and with 37% hydrochloric acid processing water to pH to being about 1.Wash organic phase twice with water, use anhydrous sodium sulfate drying.After the filtration, under vacuum, evaporate organic phase under 30 ℃/24 millibars, make 4.4 gram products thus, its fusing point after crystallization from hexanaphthene/methylene dichloride is 63-65 ℃, and its NMR and MS meet the feature of desired product.
Embodiment 12-3,4-methylene-dioxy phenol synthetic
With 17.7 gram (100 mmole) 1-(1,3-benzo dioxolane (benzodioxol)-5-yl)-and the mixture heating up to 40 of single hydration tosic acid of 1-acetone, 50 milliliters of methylene dichloride, 33.0 gram (220 mmole) 97% Tetra hydro Phthalic anhydrides and 0.42 gram (2 mmole) ℃, add 14.0 gram (140 mmole) hydrogen peroxide then.
In case described reinforced finishing, just heated mixt 6 hours under backflow.
With the reaction mixture cooling, unreacted Tetra hydro Phthalic anhydride is filtered, handle the organic solution that makes with the reactant of same amount as described in example 11 above.Make 4.3 gram products, its fusing point after crystallization from hexanaphthene/methylene dichloride is 63-65 ℃, and its NMR and MS meet the feature of desired product.
Embodiment 13-3,4-methylene-dioxy phenol synthetic
With 17.7 gram (100 mmole) 1-(1,3-benzo dioxolane (benzodioxol)-5-yl)-and the mixture heating up to 40 of single hydration tosic acid of 1-acetone, 50 milliliters of methylene dichloride, 21.4 gram (218 mmole) maleic anhydrides and 0.42 gram (2 mmole) ℃, slowly add 14.0 gram (140 mmole) hydrogen peroxide then.
In case described reinforced finishing, just heated mixt 6 hours under refluxing cools off it subsequently, and handles with the reactant of same amount like that as described in example 11 above.
Make 6.3 gram products, its fusing point after crystallization from hexanaphthene/methylene dichloride is 63-65 ℃, and its NMR and MS meet the feature of desired product.
Embodiment 14-3,4-methylene-dioxy phenol synthetic
With the mixture heating up to 40 of 17.7 gram (100 mmole) 1-(1,3-benzo dioxolane (benzodioxol)-5-yl)-1-acetone and 30 milliliters of methylene dichloride ℃; Slowly add 40.0 gram (122 mmole) phthalimidos then and cross the solution of oxy hexanoic acid (from the P.A.P. of Solvay) (purity 84.7%w/w) in 100 milliliters of methylene dichloride.
In case reinforced finishing, just with mixture heating up to refluxing 10 hours.
Subsequently it is cooled off, and handle with an amount of reactant like that as described in example 11 above.
Make 6.4 gram products, its fusing point after crystallization from hexanaphthene/methylene dichloride is 64-65 ℃, and its NMR and MS meet the feature of desired product.
Claims (40)
1. the method for the alkoxyl group phenol of preparation formula (III) and aryloxy phenol:
X wherein
1And X
2Identical or different, be straight or branched C
1-C
8Alkyl, unsubstituted or by C
1-C
8Alkyl, by trifluoromethyl or the C that replaced by halogen
6-C
10Aryl, or (OX
1) n and (OX
2) m is equivalent to group O-T-O together, T is CH herein
2, CH
2CH
2Or C (Me)
2N and m are 0,1 or 2, and its condition is not for they are 0 all the time when n=m, and this method may further comprise the steps:
A) use by corresponding organic acid and hydroperoxidation and the compound of peracid oxidation-type (I) in inert organic solvents of preparation in advance or on-site preparation:
To make the ester of corresponding formula (II);
X wherein
1, X
2, n, m such as above definition, and R is straight or branched C
2-C
6Alkyl or cycloalkyl
B) the ester hydrolysis that makes formula (II) to be making the phenol of corresponding formula (III),
In the preparation of wherein said organic peracid the concentration of used described hydrogen peroxide by weight/volume counts 30-35%.
2. the method for claim 1, wherein X
1And X
2Be C
1-C
4Alkyl.
3. as claim 1 or 2 each described methods, the T in the wherein said O-T-O group is CH
2
4. method as claimed in claim 3 is characterized in that R is C
2-C
3Alkyl.
5. method as claimed in claim 3 is characterized in that X
1And X
2For unsubstituted or by C
1-C
2The C that alkyl replaces
6Aryl.
6. method as claimed in claim 4 is characterized in that R is an ethyl.
7. method as claimed in claim 3 is characterized in that in the oxidizing reaction of step (a), and the peracid of on-site preparation is selected from by peroxyformic acid, peracetic acid, crosses toxilic acid, peroxybenzoic acid and cross the group that phthalic acid is formed.
8. method as claimed in claim 7 is characterized in that described peracid is the peroxyformic acid by formic acid and hydroperoxidation on-site preparation.
9. method as claimed in claim 8, the amount that it is characterized in that used acid are every mole of ketone 1.5 to 8 equivalents.
10. method as claimed in claim 9, the amount that it is characterized in that described acid are every mole of ketone 2 to 5 equivalents.
11. method as claimed in claim 10, the amount that it is characterized in that used hydrogen peroxide are every mole of ketone 1 to 6 equivalent.
12. method as claimed in claim 11, the amount that it is characterized in that described hydrogen peroxide are every mole of ketone 1.2 to 3 equivalents.
13. method as claimed in claim 3, it is characterized in that with the water unmixing, and the solvent of ketone that can dissolution type (I) and carboxylic acid or corresponding peracid in carry out described reaction.
14. method as claimed in claim 13 is characterized in that described solvent is selected from pentane, hexane, heptane, octane and their mixture, methylene dichloride, chloroform, tetracol phenixin and ethylene dichloride.
15. method as claimed in claim 14 is characterized in that described solvent is a chlorating.
16. method as claimed in claim 15 is characterized in that described solvent is a methylene dichloride.
17. method as claimed in claim 3 is characterized in that the pairing solvent volume of ketone of every mole of formula (I) of using rises between 1.5 liters 0.05 in step (a).
18. method as claimed in claim 17 is characterized in that described volume rises between 0.5 liter 0.2.
19. method as claimed in claim 8, the concentration that it is characterized in that described formic acid by weight/the weight meter is higher than 80%.
20. method as claimed in claim 19, the concentration that it is characterized in that described formic acid by weight/the weight meter is higher than 85%.
21. method as claimed in claim 3 is characterized in that oxidizing reaction carries out between 20 ℃ to 80 ℃.
22. method as claimed in claim 21 is characterized in that described temperature is between 30 to 50 ℃.
23. method as claimed in claim 22 is characterized in that described temperature is between 40 to 50 ℃.
24. method as claimed in claim 3 is characterized in that the hydrolysis reaction of step (b) carries out in alkalescence or sour environment.
25. method as claimed in claim 3 is characterized in that using and the identical inert solvent of solvent for use in the reaction of step (a) in step (b).
26. method as claimed in claim 25 is characterized in that the identical reaction mixture that step (a) generates uses after removing water.
27. method as claimed in claim 26 is characterized in that carrying out the hydrolysis reaction in the alkaline environment under having the situation of phase-transfer catalyst.
28. method as claimed in claim 27 is characterized in that described catalyzer is tetrabutylammonium chloride or Aliquat 360.
29. method as claimed in claim 28 is characterized in that described phase-transfer catalyst preferably adds with the mol ratio of the ester 1/20 to 1/90 of every mole of formula (II).
30. method as claimed in claim 29 is characterized in that described mol ratio is between 1/40 to 1/80.
31. method as claimed in claim 24 is characterized in that in sour environment, at C
1-C
10Carry out described reaction in the alcoholic solvent.
32. method as claimed in claim 31 is characterized in that described alcohol is C
1-C
3Alcohol.
33. method as claimed in claim 32 is characterized in that described alcohol is methyl alcohol.
34. method as claimed in claim 24 is characterized in that hydrolysis reaction carries out between 30 to 60 ℃.
35. method as claimed in claim 34, it is characterized in that this is reflected under 40 ℃ carries out.
36. method as claimed in claim 24 is characterized in that the alkoxyl group phenol of the formula (III) that generated by acidic hydrolysis or the separation of aryloxy phenol adopt the method that comprises the steps to carry out:
A) reduction vaporization methyl alcohol;
B) dissolve residuum once more with methylene dichloride, and add the sodium hydroxide solution of 2M; Removal contains the organic phase of ketone and unreacted ester;
C) aqueous phase as acidified of sodium salt of phenol that will contain formula (III) with organic or inorganic acid is used dichloromethane extraction with the alkoxyl group phenol or the aryloxy phenol of release type (III) with it;
D) with methylene dichloride evaporation to obtain residue, then with its distillation and/or crystallization to make alkoxyl group phenol or aryloxy phenol.
37. method as claimed in claim 24 is characterized in that in step (b) adopting the method that comprises following operation steps to carry out separating of the alkoxyl group phenol of the formula (III) that generated by alkaline hydrolysis or aryloxy phenol and reaction mixture:
A ') two with reaction mixture are separated; Removal contains unreacted ketone, unhydrolysed ester and the organic phase of the catalyzer that may exist;
B ') aqueous phase as acidified of sodium salt that will contain the alkoxyl group phenol of formula (III) or aryloxy phenol with strong inorganic acid is used dichloromethane extraction to discharge the corresponding phenolic derivative with it.
C ') methylene dichloride is evaporated up to obtaining residue, then with residue distillation and/or the alkoxyl group phenol and the aryloxy amphyl of crystallization to make formula (III).
38., it is characterized in that the unreacted ketone that recirculation is generated by the hydrolysis under acidic catalyst or the base catalysis in step (a) as claim 36 or 37 described methods.
39. method as claimed in claim 38 is characterized in that when described reaction mixture was to be produced by acidic hydrolysis, then the recirculation Accessory Right required 36 the middle organic phase of removing of step (B).
40. method as claimed in claim 38 is characterized in that when described reaction mixture is to be produced by alkaline hydrolysis, then uses the organic phase of removing in the step (A ') of Accessory Right requirement 37.
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| ITMI20030823 ITMI20030823A1 (en) | 2003-04-18 | 2003-04-18 | ALCOHOS AND ARYOXYPHENOL PREPARATION PROCESS. |
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| CN102452910B (en) * | 2010-10-20 | 2014-09-03 | 昆明制药集团股份有限公司 | Preparation method for 3,4,5-trialkoxy phenol |
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-
2003
- 2003-04-18 IT ITMI20030823 patent/ITMI20030823A1/en unknown
-
2004
- 2004-04-07 EP EP04726167A patent/EP1638909A2/en not_active Withdrawn
- 2004-04-07 WO PCT/EP2004/050470 patent/WO2004092106A2/en active Application Filing
- 2004-04-07 CN CN 200480010413 patent/CN100467436C/en not_active Expired - Fee Related
Non-Patent Citations (2)
| Title |
|---|
| SBS*的环氧化改性及其粘接性能研究. 韦异.广西工学院学报，第12卷第4期. 2001 |
| SBS*的环氧化改性及其粘接性能研究. 韦异.广西工学院学报，第12卷第4期. 2001 * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1638909A2 (en) | 2006-03-29 |
| ITMI20030823A1 (en) | 2004-10-19 |
| WO2004092106A2 (en) | 2004-10-28 |
| WO2004092106A3 (en) | 2004-12-09 |
| CN1777572A (en) | 2006-05-24 |
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