ZA200103328B - Processes for the preparation of (p-chlorophenyl) propanol derivatives. - Google Patents
Processes for the preparation of (p-chlorophenyl) propanol derivatives. Download PDFInfo
- Publication number
- ZA200103328B ZA200103328B ZA200103328A ZA200103328A ZA200103328B ZA 200103328 B ZA200103328 B ZA 200103328B ZA 200103328 A ZA200103328 A ZA 200103328A ZA 200103328 A ZA200103328 A ZA 200103328A ZA 200103328 B ZA200103328 B ZA 200103328B
- Authority
- ZA
- South Africa
- Prior art keywords
- compound
- preparation
- reaction
- mol
- chlorophenyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 17
- 238000002360 preparation method Methods 0.000 title claims description 11
- TXAWBKBMGZKBNN-UHFFFAOYSA-N 1-(4-chlorophenyl)propan-1-ol Chemical class CCC(O)C1=CC=C(Cl)C=C1 TXAWBKBMGZKBNN-UHFFFAOYSA-N 0.000 title description 2
- -1 alcohol compound Chemical class 0.000 claims description 20
- 150000001875 compounds Chemical class 0.000 claims description 19
- 238000005859 coupling reaction Methods 0.000 claims description 11
- 230000008878 coupling Effects 0.000 claims description 9
- 238000010168 coupling process Methods 0.000 claims description 9
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 claims description 8
- GWQSENYKCGJTRI-UHFFFAOYSA-N 1-chloro-4-iodobenzene Chemical compound ClC1=CC=C(I)C=C1 GWQSENYKCGJTRI-UHFFFAOYSA-N 0.000 claims description 7
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
- 238000006243 chemical reaction Methods 0.000 description 16
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium on carbon Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 6
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 150000001299 aldehydes Chemical class 0.000 description 4
- 238000005893 bromination reaction Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000031709 bromination Effects 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
- 229910000033 sodium borohydride Inorganic materials 0.000 description 3
- 239000012279 sodium borohydride Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 2
- 101150065749 Churc1 gene Proteins 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 102100038239 Protein Churchill Human genes 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000000702 anti-platelet effect Effects 0.000 description 2
- 239000003146 anticoagulant agent Substances 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 238000006298 dechlorination reaction Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
- OVXYDNVSUOXGQG-UHFFFAOYSA-N 1-(3-bromopropyl)-4-chlorobenzene Chemical compound ClC1=CC=C(CCCBr)C=C1 OVXYDNVSUOXGQG-UHFFFAOYSA-N 0.000 description 1
- AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical compound OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 description 1
- GXLIFJYFGMHYDY-UHFFFAOYSA-N 3-(4-chlorophenyl)prop-2-enoic acid Chemical class OC(=O)C=CC1=CC=C(Cl)C=C1 GXLIFJYFGMHYDY-UHFFFAOYSA-N 0.000 description 1
- ZHBIWFGGIKFSHZ-UHFFFAOYSA-N 3-(4-chlorophenyl)propan-1-ol Chemical compound OCCCC1=CC=C(Cl)C=C1 ZHBIWFGGIKFSHZ-UHFFFAOYSA-N 0.000 description 1
- UXIFTAZOVKVCBX-UHFFFAOYSA-N 3-(4-chlorophenyl)propanal Chemical compound ClC1=CC=C(CCC=O)C=C1 UXIFTAZOVKVCBX-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical class [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- HDOUGSFASVGDCS-UHFFFAOYSA-N pyridin-3-ylmethanamine Chemical compound NCC1=CC=CN=C1 HDOUGSFASVGDCS-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/16—Preparation of halogenated hydrocarbons by replacement by halogens of hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
- C07C45/512—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being a free hydroxyl group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP35252998 | 1998-12-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200103328B true ZA200103328B (en) | 2001-10-25 |
Family
ID=18424696
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200103328A ZA200103328B (en) | 1998-12-11 | 2001-04-24 | Processes for the preparation of (p-chlorophenyl) propanol derivatives. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US6407298B1 (cs) |
| EP (1) | EP1138660A4 (cs) |
| JP (1) | JP4474773B2 (cs) |
| KR (1) | KR20010086010A (cs) |
| CN (1) | CN1329586A (cs) |
| AU (1) | AU755010B2 (cs) |
| CA (1) | CA2347813A1 (cs) |
| CZ (1) | CZ20011368A3 (cs) |
| IL (1) | IL143665A0 (cs) |
| NO (1) | NO20012811D0 (cs) |
| NZ (1) | NZ511022A (cs) |
| SK (1) | SK6952001A3 (cs) |
| TW (1) | TW538027B (cs) |
| UA (1) | UA52841C2 (cs) |
| WO (1) | WO2000035843A1 (cs) |
| ZA (1) | ZA200103328B (cs) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7935173B1 (en) | 2010-07-23 | 2011-05-03 | Metals Recovery Technology Inc. | Process for recovery of precious metals |
| CN102757318B (zh) * | 2011-04-29 | 2015-06-24 | 上海医药工业研究院 | 一种阿利克伦中间体的制备方法 |
| JP2023128936A (ja) * | 2022-03-04 | 2023-09-14 | キオクシア株式会社 | 情報処理装置及び初期辞書作成方法 |
| CN114716296B (zh) * | 2022-03-25 | 2023-12-12 | 润药仁智(北京)科技有限公司 | 一种烷基卤化物的高效卤化合成方法 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE299187C (cs) | ||||
| US2184526A (en) * | 1937-05-27 | 1939-12-26 | Du Pont | Perfume compositions and process of making the same |
| DE1132914B (de) * | 1957-05-09 | 1962-07-12 | Siegfried Ag | Verfahren zur Herstellung von Carbaminsaeureestern von Aralkyl-alkoholen |
| US3487116A (en) * | 1966-06-16 | 1969-12-30 | Engelhard Ind Inc | Method for hydrogenation of cinnamyl alcohols |
| US3663626A (en) * | 1969-05-01 | 1972-05-16 | Universal Oil Prod Co | Hydrogenation of arylaldehydes |
| SE7407449L (cs) | 1973-07-20 | 1975-01-21 | Ciba Geigy Ag | |
| US4070374A (en) * | 1975-06-16 | 1978-01-24 | Givaudan Corporation | Process for the preparation of aryl substituted aldehydes, ketones and alcohols |
| JPS5581831A (en) | 1978-12-15 | 1980-06-20 | Toray Ind Inc | Preparation of propionaldehyde derivative |
| CA1211754A (en) * | 1980-07-09 | 1986-09-23 | David Webb | Process for the production of phenyl substituted alcohols |
| JPS59163336A (ja) * | 1983-03-09 | 1984-09-14 | Nippon Petrochem Co Ltd | アルデヒドの製造法 |
| FR2623798B1 (fr) | 1987-11-26 | 1990-05-04 | Lucien Laboratoires | Derives de trifluoromethyl-1 tetralines, leur preparation et leur application pour la synthese de composes presentant des proprietes therapeutiques |
| DD299186A5 (de) * | 1990-10-01 | 1992-04-02 | E.R. Squibb U. Sons,Inc.,Us | Phenylen-7-oxabicycloheptyl-substituierte heterocycloamid-prostaglandinanaloga |
| UA59384C2 (uk) * | 1996-12-20 | 2003-09-15 | Пфайзер, Інк. | Похідні сульфонамідів та амідів як агоністи простагландину, фармацевтична композиція та способи лікування на їх основі |
-
1999
- 1999-11-29 JP JP2000588107A patent/JP4474773B2/ja not_active Expired - Lifetime
- 1999-11-29 CZ CZ20011368A patent/CZ20011368A3/cs unknown
- 1999-11-29 NZ NZ511022A patent/NZ511022A/en unknown
- 1999-11-29 SK SK695-2001A patent/SK6952001A3/sk unknown
- 1999-11-29 CN CN99814048A patent/CN1329586A/zh active Pending
- 1999-11-29 CA CA002347813A patent/CA2347813A1/en not_active Abandoned
- 1999-11-29 WO PCT/JP1999/006654 patent/WO2000035843A1/ja not_active Application Discontinuation
- 1999-11-29 UA UA2001053136A patent/UA52841C2/uk unknown
- 1999-11-29 EP EP99973408A patent/EP1138660A4/en not_active Withdrawn
- 1999-11-29 US US09/830,555 patent/US6407298B1/en not_active Expired - Fee Related
- 1999-11-29 KR KR1020017005793A patent/KR20010086010A/ko not_active Application Discontinuation
- 1999-11-29 AU AU14114/00A patent/AU755010B2/en not_active Ceased
- 1999-11-29 IL IL14366599A patent/IL143665A0/xx unknown
- 1999-12-03 TW TW088121220A patent/TW538027B/zh active
-
2001
- 2001-04-24 ZA ZA200103328A patent/ZA200103328B/en unknown
- 2001-06-07 NO NO20012811A patent/NO20012811D0/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| JP4474773B2 (ja) | 2010-06-09 |
| TW538027B (en) | 2003-06-21 |
| NO20012811L (no) | 2001-06-07 |
| UA52841C2 (uk) | 2003-01-15 |
| CZ20011368A3 (cs) | 2001-08-15 |
| NO20012811D0 (no) | 2001-06-07 |
| IL143665A0 (en) | 2002-04-21 |
| US6407298B1 (en) | 2002-06-18 |
| CN1329586A (zh) | 2002-01-02 |
| EP1138660A1 (en) | 2001-10-04 |
| WO2000035843A1 (fr) | 2000-06-22 |
| AU755010B2 (en) | 2002-11-28 |
| SK6952001A3 (en) | 2001-12-03 |
| NZ511022A (en) | 2002-06-28 |
| EP1138660A4 (en) | 2002-10-23 |
| KR20010086010A (ko) | 2001-09-07 |
| AU1411400A (en) | 2000-07-03 |
| CA2347813A1 (en) | 2000-06-22 |
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