반응식
[C:1]1([C@H:7]([NH2:10])[CH2:8][CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.C[CH2:13][O:14]CC>CCOCC>[C:1]1([C@H:7]([N:10]=[C:13]=[O:14])[CH2:8][CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1참가 물질
4
실험 절차
To a solution of 1(R)-phenylpropylamine (14.33 g, 106 mmol) in Et2O (102 mL) was added a 1.0 M solution of HCl/Et2O (212 mL, 212 mmol). The mixture was stirred for 30 min, then the crude solution was evaporated to dryness on a rotary evaporator. The resulting white hydrochloride salt was suspended in toluene (200 mL), triphosgene was added (11.67 g, 39.3 mmol) and the resulting suspension was stirred at reflux for 3 h at room temperature overnight. The reaction mixture was concentrated and the final volume adjusted to 200 mL with toluene giving a final concentration of 0.53M. The resulting isocyanate solution was used as such. An aliquot (170 mL) was concentrated to give a colorless oil.
후처리
- customthe crude solution was evaporated to dryness on a rotary evaporator
- additiontriphosgene was added (11.67 g, 39.3 mmol)
- stirringthe resulting suspension was stirred
- concentrationThe reaction mixture was concentrated
- concentrationAn aliquot (170 mL) was concentrated
- customto give a colorless oil
출처 및 근거
- ORD 기록
- ord-3d377779649647939bbbe6a1324bee03
- 출처 데이터셋
- uspto-grants-2001_04
- 특허 번호
- US06211170B1
연결된 노트
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