RU2017720C1 - Способ получения 2,6-диметил-10-метилен-4- c1 - c4 -алкоксикарбонил-2,6,11-додекатриена - Google Patents
Способ получения 2,6-диметил-10-метилен-4- c1 - c4 -алкоксикарбонил-2,6,11-додекатриена Download PDFInfo
- Publication number
- RU2017720C1 RU2017720C1 SU843813106A SU3813106A RU2017720C1 RU 2017720 C1 RU2017720 C1 RU 2017720C1 SU 843813106 A SU843813106 A SU 843813106A SU 3813106 A SU3813106 A SU 3813106A RU 2017720 C1 RU2017720 C1 RU 2017720C1
- Authority
- RU
- Russia
- Prior art keywords
- methylene
- dimethyl
- denotes
- dodecatriene
- spectrum
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 4
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 claims description 6
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 claims description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- UQBVCZWNPCCZMC-UHFFFAOYSA-N 3-chloro-2-methyl-6-methylideneocta-1,7-diene Chemical compound CC(=C)C(Cl)CCC(=C)C=C UQBVCZWNPCCZMC-UHFFFAOYSA-N 0.000 claims description 2
- 229940043279 diisopropylamine Drugs 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- CQJHAULYLJXJNL-UHFFFAOYSA-N 4-methylpent-3-enoic acid Chemical compound CC(C)=CCC(O)=O CQJHAULYLJXJNL-UHFFFAOYSA-N 0.000 claims 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical group C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 claims 2
- 150000001450 anions Chemical class 0.000 claims 1
- 239000000010 aprotic solvent Substances 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 abstract description 10
- 229930003427 Vitamin E Natural products 0.000 abstract description 5
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 abstract description 5
- 229940046009 vitamin E Drugs 0.000 abstract description 5
- 235000019165 vitamin E Nutrition 0.000 abstract description 5
- 239000011709 vitamin E Substances 0.000 abstract description 5
- 230000015572 biosynthetic process Effects 0.000 abstract description 4
- 238000003786 synthesis reaction Methods 0.000 abstract description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000002329 infrared spectrum Methods 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 238000001819 mass spectrum Methods 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000001228 spectrum Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000001914 filtration Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000012074 organic phase Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- IMQLKJBTEOYOSI-UHFFFAOYSA-N Diphosphoinositol tetrakisphosphate Chemical compound OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 description 3
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000012300 argon atmosphere Substances 0.000 description 3
- WHWDWIHXSPCOKZ-UHFFFAOYSA-N hexahydrofarnesyl acetone Natural products CC(C)CCCC(C)CCCC(C)CCCC(C)=O WHWDWIHXSPCOKZ-UHFFFAOYSA-N 0.000 description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 3
- 235000019341 magnesium sulphate Nutrition 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 1
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- WRQNANDWMGAFTP-UHFFFAOYSA-N Methylacetoacetic acid Chemical compound COC(=O)CC(C)=O WRQNANDWMGAFTP-UHFFFAOYSA-N 0.000 description 1
- 101150003085 Pdcl gene Proteins 0.000 description 1
- VYBREYKSZAROCT-UHFFFAOYSA-N alpha-myrcene Natural products CC(=C)CCCC(=C)C=C VYBREYKSZAROCT-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- -1 ethyl 4-methyl-3-pentenoic acid Chemical compound 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- MYAJTCUQMQREFZ-UHFFFAOYSA-K tppts Chemical compound [Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC=CC(P(C=2C=C(C=CC=2)S([O-])(=O)=O)C=2C=C(C=CC=2)S([O-])(=O)=O)=C1 MYAJTCUQMQREFZ-UHFFFAOYSA-K 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/185—Saturated compounds having only one carboxyl group and containing keto groups
-
- 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
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/673—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by change of size of the carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8318392A FR2555170B1 (fr) | 1983-11-18 | 1983-11-18 | Nouveaux derives insatures, leur preparation et leur emploi |
| FR8318392 | 1983-11-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2017720C1 true RU2017720C1 (ru) | 1994-08-15 |
Family
ID=9294282
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU843813106A RU2017720C1 (ru) | 1983-11-18 | 1984-11-16 | Способ получения 2,6-диметил-10-метилен-4- c1 - c4 -алкоксикарбонил-2,6,11-додекатриена |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US4615838A (https=) |
| EP (1) | EP0145555B1 (https=) |
| JP (1) | JPS60116640A (https=) |
| AT (1) | ATE23147T1 (https=) |
| CA (1) | CA1250312A (https=) |
| DE (1) | DE3461079D1 (https=) |
| FR (1) | FR2555170B1 (https=) |
| RU (1) | RU2017720C1 (https=) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2034261A1 (en) * | 1990-01-17 | 1991-07-18 | Mitsubishi Chemical Corporation | Acyclic terpenes |
| US5298655A (en) * | 1991-09-27 | 1994-03-29 | Merck & Co., Inc. | Farnesyl pyrophosphate analogs |
| US5574025A (en) * | 1994-10-26 | 1996-11-12 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferases |
| EP1327620A1 (en) * | 2002-01-14 | 2003-07-16 | Aventis Animal Nutrition S.A. | Process for the preparation of phytone |
| US20100121057A1 (en) * | 2007-04-17 | 2010-05-13 | Merck Serono Sa | Process for the Preparation of Piperazine Benzothiazoles |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1008729B (de) * | 1955-06-02 | 1957-05-23 | Basf Ag | Verfahren zur Herstellung von konjugiert-ungesaettigten Oxocarbonsaeureestern |
| US3032491A (en) * | 1958-07-23 | 1962-05-01 | Polaroid Corp | Irradiation of cyclohexadienones |
| US3781313A (en) * | 1971-01-20 | 1973-12-25 | Rhone Poulenc Sa | Sulfone intermediates for the synthesis of vitamin a |
| US4016178A (en) * | 1975-06-17 | 1977-04-05 | Hoffmann-La Roche Inc. | Synthesis of vitamin E |
| JPS601283B2 (ja) * | 1976-06-08 | 1985-01-14 | 帝人株式会社 | 包接化合物並びにその製造法 |
| US4221742A (en) * | 1977-12-29 | 1980-09-09 | Scm Corporation | Coupling reaction involving a Grignard and allylic halide |
| DE3013672A1 (de) * | 1980-04-09 | 1981-10-15 | Consortium für elektrochemische Industrie GmbH, 8000 München | 2,4-dialkyl-2.6-heptadienal-derivate, verfahren zu deren herstellung und ihre anwendung als geruchs- und geschmacksstoffe |
| US4564477A (en) * | 1982-02-19 | 1986-01-14 | Kuraray Co., Ltd. | Polyprenyl compounds and method of producing the same |
-
1983
- 1983-11-18 FR FR8318392A patent/FR2555170B1/fr not_active Expired
-
1984
- 1984-11-13 DE DE8484402298T patent/DE3461079D1/de not_active Expired
- 1984-11-13 AT AT84402298T patent/ATE23147T1/de not_active IP Right Cessation
- 1984-11-13 EP EP84402298A patent/EP0145555B1/fr not_active Expired
- 1984-11-15 CA CA000467918A patent/CA1250312A/fr not_active Expired
- 1984-11-16 JP JP59242209A patent/JPS60116640A/ja active Granted
- 1984-11-16 RU SU843813106A patent/RU2017720C1/ru active
- 1984-11-16 US US06/671,963 patent/US4615838A/en not_active Expired - Fee Related
-
1985
- 1985-09-13 US US06/775,835 patent/US4693849A/en not_active Expired - Fee Related
Non-Patent Citations (1)
| Title |
|---|
| ЕПВ N 0044771, кл. B 01J 31/24, 1982. * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0145555B1 (fr) | 1986-10-29 |
| JPS60116640A (ja) | 1985-06-24 |
| JPH058689B2 (https=) | 1993-02-02 |
| CA1250312A (fr) | 1989-02-21 |
| FR2555170B1 (fr) | 1986-07-18 |
| DE3461079D1 (en) | 1986-12-04 |
| US4693849A (en) | 1987-09-15 |
| ATE23147T1 (de) | 1986-11-15 |
| FR2555170A1 (fr) | 1985-05-24 |
| US4615838A (en) | 1986-10-07 |
| EP0145555A3 (en) | 1985-08-07 |
| EP0145555A2 (fr) | 1985-06-19 |
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