JPH034049B2 - - Google Patents
Info
- Publication number
- JPH034049B2 JPH034049B2 JP3325783A JP3325783A JPH034049B2 JP H034049 B2 JPH034049 B2 JP H034049B2 JP 3325783 A JP3325783 A JP 3325783A JP 3325783 A JP3325783 A JP 3325783A JP H034049 B2 JPH034049 B2 JP H034049B2
- Authority
- JP
- Japan
- Prior art keywords
- hydroxy
- present
- acid
- amine salt
- salt
- 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
- 150000003947 ethylamines Chemical class 0.000 claims 1
- -1 hydroxy acid methyl ester Chemical class 0.000 description 17
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- WQNCWSOLWQSLRJ-UHFFFAOYSA-N 4-hydroxytetradec-5-ynoic acid Chemical compound CCCCCCCCC#CC(O)CCC(O)=O WQNCWSOLWQSLRJ-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 230000003287 optical effect Effects 0.000 description 7
- RTCUCQWIICFPOD-SECBINFHSA-N (1r)-1-naphthalen-1-ylethanamine Chemical compound C1=CC=C2C([C@H](N)C)=CC=CC2=C1 RTCUCQWIICFPOD-SECBINFHSA-N 0.000 description 6
- 239000003016 pheromone Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 5
- 244000046052 Phaseolus vulgaris Species 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- RUJHATQMIMUYKD-UHFFFAOYSA-N 2-naphthalen-1-ylethanamine Chemical class C1=CC=C2C(CCN)=CC=CC2=C1 RUJHATQMIMUYKD-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 150000001261 hydroxy acids Chemical class 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical group CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
- 230000002194 synthesizing effect Effects 0.000 description 3
- SYTBZMRGLBWNTM-SNVBAGLBSA-N (R)-flurbiprofen Chemical class FC1=CC([C@H](C(O)=O)C)=CC=C1C1=CC=CC=C1 SYTBZMRGLBWNTM-SNVBAGLBSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- BHHGXPLMPWCGHP-UHFFFAOYSA-N Phenethylamine Chemical compound NCCC1=CC=CC=C1 BHHGXPLMPWCGHP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 210000003786 sclera Anatomy 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- RHOQRBVFJSAQTR-UHFFFAOYSA-N tetradec-5-ynoic acid Chemical compound CCCCCCCCC#CCCCC(O)=O RHOQRBVFJSAQTR-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3325783A JPS59157052A (ja) | 1983-02-28 | 1983-02-28 | 新規なナフチルエチルアミン誘導体 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3325783A JPS59157052A (ja) | 1983-02-28 | 1983-02-28 | 新規なナフチルエチルアミン誘導体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59157052A JPS59157052A (ja) | 1984-09-06 |
| JPH034049B2 true JPH034049B2 (sv) | 1991-01-22 |
Family
ID=12381448
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3325783A Granted JPS59157052A (ja) | 1983-02-28 | 1983-02-28 | 新規なナフチルエチルアミン誘導体 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59157052A (sv) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104447294A (zh) * | 2014-11-24 | 2015-03-25 | 苏州乔纳森新材料科技有限公司 | 一种3-环己烯-1-甲酸的手性拆分方法 |
-
1983
- 1983-02-28 JP JP3325783A patent/JPS59157052A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59157052A (ja) | 1984-09-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR100284216B1 (ko) | 플로르페니콜, 티암페니콜, 클로람페니콜 및 옥사졸린 중간체의 비대칭적 제조방법 | |
| EP1200384B1 (de) | 2-alkyl-5-halogen-pent-4-encarbonsäuren und deren herstellung | |
| Legters et al. | Synthesis of naturally occurring (2S, 3S)-(+)-aziridine-2, 3-dicarboxylic acid. | |
| JPH11130710A (ja) | パラ−メンタン−３，８−ジオールの製造方法 | |
| CA1265819A (en) | Method for preparing ( )r-2-methyl-hexane-1,2-diol | |
| CH627432A5 (en) | Process for the preparation of vinylcyclopropanecarboxylates | |
| KR0144684B1 (ko) | 디카르복실산의 모노에스테르 및 그의 제조방법 | |
| JPS6215057B2 (sv) | ||
| JPH034049B2 (sv) | ||
| KR940011907B1 (ko) | α-(1-메틸에틸)-3,4-디메톡시벤젠아세토니트릴의 새로운 제조방법 | |
| CA1123006A (en) | Preparation of cyclopropane derivatives | |
| SU1083906A3 (ru) | Способ получени фениловых сложных эфиров карбаминовой кислоты | |
| US4408066A (en) | Methyl cyclopropane-1,3-dicarboxylate | |
| SU1169527A3 (ru) | Способ получени хлорформиатов @ - @ -алкиловых эфиров @ - @ - @ -алкилтартроновой кислоты | |
| RU2058979C1 (ru) | Производные алкенкарбоновой кислоты, или смеси их изомеров, или их индивидуальные изомеры, или соли, обладающие свойствами антагонистов лейкотриена, способы их получения, промежуточные для их получения, и фармацевтическая композиция на их основе | |
| US4170596A (en) | Novel monoesters of cis-cyclopentenediol, process for preparation thereof, and process for preparation of lactones from the monoesters | |
| JP3081854B2 (ja) | 光学活性なレボブノロール合成中間体の製造方法 | |
| US4211720A (en) | Preparation of cyano-substituted cyclopropane derivatives | |
| JP4661272B2 (ja) | キラルな４−メチル−４−［（アリールカルボオキシ）エチル］−オキセタン−２−オンおよびキラルメバロノラクトンの製造方法 | |
| JP2562955B2 (ja) | （Ｒ）―４―ヒドロキシ―５―テトラデシン酸―（Ｒ）―（＋）―α―（１―ナフチル）エチルアミン塩の製造方法 | |
| SU331541A1 (ru) | Шскм библиотека | |
| SU1201279A1 (ru) | Способ получени 2-производных адамантана | |
| KR100449750B1 (ko) | 라세믹 알킬 4-클로로-3-히드록시부티레이트의 제조방법 | |
| JP4064645B2 (ja) | 多置換シクロアルケン類の新規製造法 | |
| KR100441137B1 (ko) | 키랄 2,2-디메틸시클로프로판카르복실의 유도체의 제조방법 |