DE2719916C2 - Verfahren zur Herstellung von 2,9-Dioxatricyclo[4,3,1,0↑3↑↑,↑↑7↑]decanen - Google Patents
Verfahren zur Herstellung von 2,9-Dioxatricyclo[4,3,1,0↑3↑↑,↑↑7↑]decanenInfo
- Publication number
- DE2719916C2 DE2719916C2 DE2719916A DE2719916A DE2719916C2 DE 2719916 C2 DE2719916 C2 DE 2719916C2 DE 2719916 A DE2719916 A DE 2719916A DE 2719916 A DE2719916 A DE 2719916A DE 2719916 C2 DE2719916 C2 DE 2719916C2
- Authority
- DE
- Germany
- Prior art keywords
- hoch
- general formula
- hydrogen
- beta
- uarr
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000002360 preparation method Methods 0.000 title claims description 12
- 238000000034 method Methods 0.000 title claims description 7
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 38
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 10
- 150000002431 hydrogen Chemical class 0.000 claims description 9
- 239000011541 reaction mixture Substances 0.000 claims description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 239000000741 silica gel Substances 0.000 claims description 5
- 229910002027 silica gel Inorganic materials 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 4
- 150000001540 azides Chemical class 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000002425 crystallisation Methods 0.000 claims description 4
- 230000008025 crystallization Effects 0.000 claims description 4
- 238000001704 evaporation Methods 0.000 claims description 4
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims description 2
- 239000002585 base Substances 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 238000004587 chromatography analysis Methods 0.000 claims description 2
- 238000007327 hydrogenolysis reaction Methods 0.000 claims description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 229910003446 platinum oxide Inorganic materials 0.000 claims description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 230000008020 evaporation Effects 0.000 claims 1
- 238000007098 aminolysis reaction Methods 0.000 description 10
- FEWJPZIEWOKRBE-JCYAYHJZSA-M L-tartrate(1-) Chemical compound OC(=O)[C@H](O)[C@@H](O)C([O-])=O FEWJPZIEWOKRBE-JCYAYHJZSA-M 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000013078 crystal Substances 0.000 description 5
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- WDYVUKGVKRZQNM-UHFFFAOYSA-N 6-phosphonohexylphosphonic acid Chemical compound OP(O)(=O)CCCCCCP(O)(O)=O WDYVUKGVKRZQNM-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- 239000001358 L(+)-tartaric acid Substances 0.000 description 2
- 235000011002 L(+)-tartaric acid Nutrition 0.000 description 2
- FEWJPZIEWOKRBE-LWMBPPNESA-N L-(+)-Tartaric acid Natural products OC(=O)[C@@H](O)[C@H](O)C(O)=O FEWJPZIEWOKRBE-LWMBPPNESA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-M 3-carboxy-2,3-dihydroxypropanoate Chemical compound OC(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-M 0.000 description 1
- -1 N'-substituted piperazine Chemical class 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- MKJDUHZPLQYUCB-UHFFFAOYSA-N decan-4-one Chemical compound CCCCCCC(=O)CCC MKJDUHZPLQYUCB-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000000803 paradoxical effect Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/08—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (26)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2719916A DE2719916C2 (de) | 1977-05-04 | 1977-05-04 | Verfahren zur Herstellung von 2,9-Dioxatricyclo[4,3,1,0↑3↑↑,↑↑7↑]decanen |
| NO771806A NO146360C (no) | 1977-05-04 | 1977-05-24 | Fremgangsmaate ved fremstilling av 10alfa- og 10beta-methyl-2,9-dioxatricyclo-(4.3.1.03,7)-decaner |
| GR53578A GR70658B (US07816562-20101019-C00012.png) | 1977-05-04 | 1977-05-28 | |
| NL7706640A NL7706640A (nl) | 1977-05-04 | 1977-06-16 | Werkwijze voor de bereiding van 2,9-dioxatri- cyclo(4,3,1,03-,7)decanen. |
| DK273977A DK273977A (da) | 1977-05-04 | 1977-06-21 | Fremgangsmaade til fremstilling af 2,9-dioxatricyclo (4,3,1,03, 7) decan-forbindelser |
| GB29095/77A GB1581263A (en) | 1977-05-04 | 1977-07-11 | Process for the production of 2,9-dioxatricyclo (4,3,1,03,7) decanes |
| IE1428/77A IE45756B1 (en) | 1977-05-04 | 1977-07-11 | Improvements in and relating to a process for the production of 2,9-dioxatricyclo (4,3,1,03,7) decanes |
| IL52539A IL52539A (en) | 1977-02-14 | 1977-07-15 | Preparation of 2,9-dioxytricyclo (4,3,1,03,7)decanes |
| MX77100803U MX4851E (es) | 1977-05-04 | 1977-07-21 | Procedimiento para obtener 2,9-dioxatriciclo (4,3,1,03,7)decano |
| AT554377A AT352139B (de) | 1977-05-04 | 1977-07-28 | Verfahren zur herstellung von neuen 2,9- dioxatricyclo-(4,3,1,03,7)decanen und deren salzen |
| ES461131A ES461131A2 (es) | 1977-05-04 | 1977-07-29 | Procedimiento para la preparacion de 2,9-dioxatriciclo (4,3,1,0,3,7)decanos. |
| ZA00774753A ZA774753B (en) | 1977-05-04 | 1977-08-05 | Process for the manufacture of 2,9-dioxatricyclo(4,3,1,3 3'7)decanen |
| CH971477A CH638213A5 (de) | 1977-05-04 | 1977-08-08 | Verfahren zur herstellung von 2,9-dioxatricyclo-(4,3,1,03,7)-decanen. |
| CA284,645A CA1130300A (en) | 1977-05-04 | 1977-08-09 | Process for preparing 10-methyl-2,9- dioxatricyclo [4,3,1,0 su3,7 xx] decanes |
| AU27794/77A AU512406B2 (en) | 1977-05-04 | 1977-08-10 | A process for the production of 2, 9 -dixatricyclo-[4,3,1,03,7] decanes |
| NZ184901A NZ184901A (en) | 1977-02-14 | 1977-08-11 | Production of 2,9-dioxatricyclo(4,3,1,03,1) decane derivatives |
| JP9771777A JPS53137995A (en) | 1977-05-04 | 1977-08-15 | Process for preparing 2*99dioxatricyclo*4*3*1*03*7*decane |
| DD7700200649A DD132871A6 (de) | 1977-05-04 | 1977-08-18 | Verfahren zur herstellung von 2,9-dioxatricyclo eckige klammer auf 4,3,1,0 hoch 3,7 eckige klammer zu decanen |
| SE7709317A SE439310B (sv) | 1977-05-04 | 1977-08-18 | Sett att framstella 2,9-dioxatricyklo(4,3,1,0?723?72,?727)dekaner |
| SU772511707A SU724084A3 (ru) | 1977-05-04 | 1977-08-19 | Способ получени 10 -метил- или 10 -метил-2,9-диоксатрицикло (4,3,1,03,7) деканов или их солей |
| BE6046120A BE857981R (fr) | 1977-05-04 | 1977-08-19 | 2,9-dioxatricyclo (4,3,1,0 3,7) decanes et procede pour leur preparation |
| FI772488A FI772488A (fi) | 1977-05-04 | 1977-08-19 | Foerfarande foer framstaellning av 2,9-dioxatricyklo(4,3,1,03,7)-dekaner |
| FR7725388A FR2389628B2 (US07816562-20101019-C00012.png) | 1977-05-04 | 1977-08-19 | |
| US05/826,636 US4182889A (en) | 1977-05-04 | 1977-08-22 | Process for preparing 10-methyl-2,9-dioxatricyclo[4,3,1,03,7 ] decanes |
| PH20155A PH15677A (en) | 1977-05-04 | 1977-08-22 | Process for the production of 2,9-dioxatricyclo(4,3,1,0 3)decanes |
| JP60247310A JPS61197584A (ja) | 1977-05-04 | 1985-11-06 | ２，９−ジオキサトリシクロ〔４，３，１，０↑３’↑７〕デカンの製法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2719916A DE2719916C2 (de) | 1977-05-04 | 1977-05-04 | Verfahren zur Herstellung von 2,9-Dioxatricyclo[4,3,1,0↑3↑↑,↑↑7↑]decanen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2719916A1 DE2719916A1 (de) | 1978-11-09 |
| DE2719916C2 true DE2719916C2 (de) | 1987-03-19 |
Family
ID=6007994
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2719916A Expired DE2719916C2 (de) | 1977-02-14 | 1977-05-04 | Verfahren zur Herstellung von 2,9-Dioxatricyclo[4,3,1,0↑3↑↑,↑↑7↑]decanen |
Country Status (23)
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2547205C2 (de) * | 1975-10-22 | 1983-12-08 | Kali-Chemie Pharma Gmbh, 3000 Hannover | 2,9-Dioxatricyclo[4,3,1,0↑3↑↑,↑↑7↑]decane und Verfahren zu deren Herstellung |
| DE3335826A1 (de) * | 1983-10-01 | 1985-04-18 | Kali-Chemie Pharma Gmbh, 3000 Hannover | Neue n-(2,10-dioxa-tricyclo-(5,3,1,0(pfeil hoch)3(pfeil hoch)(pfeil hoch),(pfeil hoch)(pfeil hoch)8(pfeil hoch))- undecan-5-yl)-tryptamin-derivate |
| DE3335827A1 (de) * | 1983-10-01 | 1985-04-18 | Kali-Chemie Pharma Gmbh, 3000 Hannover | Neue 2,6-dioxa-bicyclo-(2,2,2)-octan-7-yl- acetaldehyde |
| SE510643C2 (sv) * | 1997-06-27 | 1999-06-14 | Astra Ab | Termodynamiskt stabil omeprazol natrium form B |
| DE10130145A1 (de) * | 2001-06-22 | 2003-01-02 | Wella Ag | Kationische Farbstoffe, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Färbemittel |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3812154A (en) * | 1969-12-08 | 1974-05-21 | Kali Chemie Ag | Dioxatricyclodecanes |
| DE2129507C3 (de) | 1971-06-15 | 1980-02-14 | Kali-Chemie Ag, 3000 Hannover | Verfahren zur Herstellung von 8-Alkoxy-3halogenmethyl-4-acetoxy- 10-methylen-2,9dioxatricyclo(43,l,03 7 )decanen |
| FI56533C (fi) | 1973-02-08 | 1980-02-11 | Kali Chemie Pharma Gmbh | Saett att framstaella nya 4alfa-karbamyloxi-8-alkoxi-10-metylen-3-metyl-2,9-dioxatricyklo(4,3,1,03,7)-dekaner |
-
1977
- 1977-05-04 DE DE2719916A patent/DE2719916C2/de not_active Expired
- 1977-05-24 NO NO771806A patent/NO146360C/no unknown
- 1977-05-28 GR GR53578A patent/GR70658B/el unknown
- 1977-06-16 NL NL7706640A patent/NL7706640A/xx not_active Application Discontinuation
- 1977-06-21 DK DK273977A patent/DK273977A/da not_active Application Discontinuation
- 1977-07-11 IE IE1428/77A patent/IE45756B1/en unknown
- 1977-07-11 GB GB29095/77A patent/GB1581263A/en not_active Expired
- 1977-07-21 MX MX77100803U patent/MX4851E/es unknown
- 1977-07-28 AT AT554377A patent/AT352139B/de not_active IP Right Cessation
- 1977-07-29 ES ES461131A patent/ES461131A2/es not_active Expired
- 1977-08-05 ZA ZA00774753A patent/ZA774753B/xx unknown
- 1977-08-08 CH CH971477A patent/CH638213A5/de not_active IP Right Cessation
- 1977-08-09 CA CA284,645A patent/CA1130300A/en not_active Expired
- 1977-08-10 AU AU27794/77A patent/AU512406B2/en not_active Expired
- 1977-08-15 JP JP9771777A patent/JPS53137995A/ja active Pending
- 1977-08-18 DD DD7700200649A patent/DD132871A6/xx not_active IP Right Cessation
- 1977-08-18 SE SE7709317A patent/SE439310B/xx not_active IP Right Cessation
- 1977-08-19 SU SU772511707A patent/SU724084A3/ru active
- 1977-08-19 FI FI772488A patent/FI772488A/fi not_active Application Discontinuation
- 1977-08-19 FR FR7725388A patent/FR2389628B2/fr not_active Expired
- 1977-08-19 BE BE6046120A patent/BE857981R/xx not_active IP Right Cessation
- 1977-08-22 US US05/826,636 patent/US4182889A/en not_active Expired - Lifetime
- 1977-08-22 PH PH20155A patent/PH15677A/en unknown
-
1985
- 1985-11-06 JP JP60247310A patent/JPS61197584A/ja active Granted
Non-Patent Citations (1)
| Title |
|---|
| NICHTS-ERMITTELT |
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