반응식
Cl.[CH3:2][O:3][C:4](=[O:14])[C@H:5]([CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[NH2:6].N1C=CC=CC=1.[C:21](OC(=O)C)(=[O:23])[CH3:22]>>[CH3:2][O:3][C:4](=[O:14])[C@H:5]([CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[NH:6][C:21](=[O:23])[CH3:22]참가 물질
4
실험 절차
To a solution of 2.73 g of L-phenylalanine methyl ester hydrochloride (12.7 mmol) in 5.00 g of pyridine (63.2 mmol) is dropwise added 12.90 g of acetic anhydride (126.0 mmol) under ice cooling. The mixture is allowed to stand for 2 hours and concentrated in vacuo. The residue is extracted with ethyl acetate. The extract is washed with 5% hydrochloric acid, saturated aqueous sodium bicarbonate and saturated brine in order, dried over sodium sulfate, filtered and concentrated in vacuo to give 2.34 g of the objective N-acetylphenylalanine methyl ester 4. Yield, 83.6%.
후처리
- concentrationconcentrated in vacuo
- extractionThe residue is extracted with ethyl acetate
- washThe extract is washed with 5% hydrochloric acid, saturated aqueous sodium bicarbonate and saturated brine in order
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-1ce600d5419d406eb85eddbc8f83dfe6
- 출처 데이터셋
- uspto-grants-1994_07
- 특허 번호
- US05326780
연결된 노트
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