Triethylamine → (4RS,5SR)-5-(3-chlorophenyl)-4-[4-(2,2,3,3,3-pentafluoropropyl)benzyl]-1,3-oxazolidin-2-one
반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]([OH:28])[CH:9]([CH2:13][C:14]2[CH:19]=[CH:18][C:17]([CH2:20][C:21]([F:27])([F:26])[C:22]([F:25])([F:24])[F:23])=[CH:16][CH:15]=2)C(O)=O)[CH:5]=[CH:6][CH:7]=1.C([N:31]([CH2:34]C)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:43])C=CC=CC=1>O1CCCC1>[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]2[O:28][C:34](=[O:43])[NH:31][CH:9]2[CH2:13][C:14]2[CH:15]=[CH:16][C:17]([CH2:20][C:21]([F:26])([F:27])[C:22]([F:25])([F:24])[F:23])=[CH:18][CH:19]=2)[CH:5]=[CH:6][CH:7]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of (2RS,3RS)-3-(3-chlorophenyl)-3-hydroxy-2-[4-(2,2,3,3,3-pentafluoropropyl)benzyl]propionic acid (2.75 g, 6.50 mmol) in tetrahydrofuran (70 ml) were added triethylamine (1.36 ml, 9.75 mmol) and diphenylphosphoryl azide (1.54 ml, 7.15 mmol), and the mixture was heated under reflux for 4 hrs. The solvent was evaporated and the residue was diluted with ethyl acetate, washed with water, saturated. aqueous sodium hydrogen carbonate and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue as recrystallized from hexane-ethyl acetate to give (4RS,5SR)-5-(3-chlorophenyl)-4-[4-(2,2,3,3,3-pentafluoropropyl)benzyl]-1,3-oxazolidin-2-one (2.54 g, 93%) as colorless crystals.
후처리
- temperaturethe mixture was heated
- temperatureunder reflux for 4 hrs
- customThe solvent was evaporated
- additionthe residue was diluted with ethyl acetate
- washwashed with water
- dry with materialThe organic layer was dried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe residue as recrystallized from hexane-ethyl acetate
출처 및 근거
- ORD 기록
- ord-e99d7f5fa7cb423fb6cff27aac897866
- 출처 데이터셋
- uspto-grants-2006_01
- 특허 번호
- US06982348B2
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