반응식
[C:1]([C:9]1[CH:10]=[C:11]([CH:15]([CH3:19])[C:16]([OH:18])=[O:17])[CH:12]=[CH:13][CH:14]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.COC(C)(C)C.CC(C)[C@@H](C1C=CC=CC=1)CN>O>[C:1]([C:9]1[CH:10]=[C:11]([C@H:15]([CH3:19])[C:16]([OH:18])=[O:17])[CH:12]=[CH:13][CH:14]=1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
반응 조건
- 온도
- 10 °C
실험 절차
To (±)-2-(3-benzoylphenyl)propionic acid (1200 g, 4.719 mol) were added methyl-t-butyl ether (hereinafter abbreviated to "MTBE") (4.8 L) and water (600 g, water/KET=0.50) and the mixture was dissolved with heating. Then, (S)-(+)-3-methyl-2-phenylbutylamine (388 g, 2.377 mol) was added dropwise with stirring at 50° C. to 55° C. This reaction solution was cooled to precipitate a crystal and then reheated from 35° C. to 50° C. This solution was again cooled and then reheated from 40° C. to 45° C. This solution was cooled slowly to 10° C. and stirred at 5° C. to 10° C. for one hour. Then, the crystal precipitated was filtered, and the filter cake was washed three times with cold MTBE (1 L) and dried. In this manner, a diastereomer salt (741 g, 1.775 mol) of (S)-(+)-2-(3-benzoylphenyl)propionic acid with (S)-(+)-3-methyl-2-phenylbutylamine was obtained. The yield of the product based on (S)-(+)-2-(3-benzoylphenyl)propionic acid contained in the starting material was 75.2% and the optical purity was 99.1% e.e.
후처리
- dissolutionthe mixture was dissolved
- temperaturewith heating
- temperatureThis reaction solution was cooled
- customto precipitate a crystal
- customreheated from 35° C. to 50° C
- temperatureThis solution was again cooled
- customreheated from 40° C. to 45° C
- stirringstirred at 5° C. to 10° C. for one hour
- customThen, the crystal precipitated
- filtrationwas filtered
- washthe filter cake was washed three times with cold MTBE (1 L)
- customdried
출처 및 근거
- ORD 기록
- ord-8d08a3aac40e4298a777f7c845a403bb
- 출처 데이터셋
- uspto-grants-1998_12
- 특허 번호
- US05852209
연결된 노트
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