JPS6241709B2 - - Google Patents
Info
- Publication number
- JPS6241709B2 JPS6241709B2 JP17414284A JP17414284A JPS6241709B2 JP S6241709 B2 JPS6241709 B2 JP S6241709B2 JP 17414284 A JP17414284 A JP 17414284A JP 17414284 A JP17414284 A JP 17414284A JP S6241709 B2 JPS6241709 B2 JP S6241709B2
- Authority
- JP
- Japan
- Prior art keywords
- mmol
- compound
- ethyl ether
- compounds
- alcohol
- 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
- 150000001875 compounds Chemical class 0.000 claims description 40
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 36
- -1 bicyclic terpenoids Chemical class 0.000 description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- 235000019441 ethanol Nutrition 0.000 description 12
- 239000000243 solution Substances 0.000 description 11
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 239000012267 brine Substances 0.000 description 8
- 238000001035 drying Methods 0.000 description 8
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- LUFPJJNWMYZRQE-UHFFFAOYSA-N benzylsulfanylmethylbenzene Chemical compound C=1C=CC=CC=1CSCC1=CC=CC=C1 LUFPJJNWMYZRQE-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 6
- 239000000543 intermediate Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 239000012280 lithium aluminium hydride Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- DFZMKOVWHYSLQF-DHZHZOJOSA-N (3e)-4,8-dimethylnona-3,7-dien-1-ol Chemical compound CC(C)=CCC\C(C)=C\CCO DFZMKOVWHYSLQF-DHZHZOJOSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 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 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000001819 mass spectrum Methods 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000007363 ring formation reaction Methods 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 240000000560 Citrus x paradisi Species 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- UENWRTRMUIOCKN-UHFFFAOYSA-N benzyl thiol Chemical compound SCC1=CC=CC=C1 UENWRTRMUIOCKN-UHFFFAOYSA-N 0.000 description 2
- BXQLAXIZPLEGMU-FMIVXFBMSA-N ethyl (3e)-4,8-dimethylnona-3,7-dienoate Chemical compound CCOC(=O)C\C=C(/C)CCC=C(C)C BXQLAXIZPLEGMU-FMIVXFBMSA-N 0.000 description 2
- 150000004678 hydrides Chemical class 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000012359 Methanesulfonyl chloride Substances 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000002153 concerted effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- MOUHZLCHRBYVPF-UHFFFAOYSA-N n,n-diethylethanamine;methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O.CCN(CC)CC MOUHZLCHRBYVPF-UHFFFAOYSA-N 0.000 description 1
- OUMRUWRPTBYLRS-UHFFFAOYSA-N phenylmethanethiol;sodium Chemical compound [Na].SCC1=CC=CC=C1 OUMRUWRPTBYLRS-UHFFFAOYSA-N 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17414284A JPS6153261A (ja) | 1984-08-23 | 1984-08-23 | 分鎖状含硫化合物 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17414284A JPS6153261A (ja) | 1984-08-23 | 1984-08-23 | 分鎖状含硫化合物 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6153261A JPS6153261A (ja) | 1986-03-17 |
JPS6241709B2 true JPS6241709B2 (enrdf_load_stackoverflow) | 1987-09-04 |
Family
ID=15973399
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17414284A Granted JPS6153261A (ja) | 1984-08-23 | 1984-08-23 | 分鎖状含硫化合物 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6153261A (enrdf_load_stackoverflow) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19615134C2 (de) * | 1996-04-17 | 2003-04-17 | Continental Ag | Haftvermittlersubstanz zwischen vulkanisierbarem Polymer und metallischem Festigkeitsträger, Verfahren zu deren Aufbringung sowie deren Verwendung |
-
1984
- 1984-08-23 JP JP17414284A patent/JPS6153261A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6153261A (ja) | 1986-03-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3575705B2 (ja) | ジンゲロールおよびショーガオールの製造法 | |
JPS6241709B2 (enrdf_load_stackoverflow) | ||
JP7553928B2 (ja) | ビリベルジン系化合物及びその製造方法並びに用途 | |
PL92979B1 (enrdf_load_stackoverflow) | ||
US4172076A (en) | Process for preparing steroidal acids and their intermediate derivatives | |
JPS62201842A (ja) | 3−ヒドロキシシクロペント−4−エン−1−オン類の製造法 | |
IE44083B1 (en) | Method for oxidising cinchona alkaloids | |
Murai et al. | Aldol-type condensation reactions of lithium eneselenolates generated from selenoamides with aldehydes | |
JPH0115511B2 (enrdf_load_stackoverflow) | ||
US4524221A (en) | Process for the production of acyloins | |
JP3228486B2 (ja) | ヒドロキシケトン誘導体およびその製造方法 | |
US4052434A (en) | Prostaglandin intermediates | |
US4215057A (en) | Process for the production of substituted furans | |
US4454351A (en) | Lactonic derivatives and use of same as starting materials for the preparation of macrocyclic hydroxyketones | |
FI90068B (fi) | Foerfarande foer framstaellning av a-vitamin eller dess karboxylsyraestrar | |
JPH07145098A (ja) | アルコキシル基含有化合物 | |
JPH072678B2 (ja) | 2−シクロペンテノン誘導体の製造法 | |
JPH0348909B2 (enrdf_load_stackoverflow) | ||
JP2542843B2 (ja) | 新規なノルボルナン誘導体およびその製造法 | |
JPS58170726A (ja) | メタアクロレンアセタ−ルを原料とするジヒドロタゲトンの製造法 | |
JPH0262548B2 (enrdf_load_stackoverflow) | ||
US4556723A (en) | Process for the production of acyloins | |
JPH039893B2 (enrdf_load_stackoverflow) | ||
JPH07126285A (ja) | ステロイド誘導体の製造方法 | |
JPH0421654B2 (enrdf_load_stackoverflow) |