반응식
C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[CH2:15]([NH2:23])[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.[C:24]1([CH2:30][CH:31]=O)[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.OP([O-])(O)=O.[K+]>CO>[CH2:15]([NH:23][CH2:31][CH2:30][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1참가 물질
6
실험 절차
Sodiumtriacetoxyborohydride (8.87 g, 41.3 mmol) is added in small portions at 0° C. to a stirred solution of phenethylamine (5.0 g, 41.3 mmol) and phenylacetaldehyde (4.96 g, 41.3 mmol) in methanol (50 ml). The reaction mixture is stirred at rt overnight, poured onto saturated aqueous KH2PO4 solution and extracted twice with EtOAc. The solvent is evaporated, the residue is taken up in 1N HCl and washed twice with dichloromethane. The aqueous layer is adjusted to pH 9 by the addition of ammonium hydroxide solution and extracted with dichloromethane. Drying the combined organic layers over Na2SO4 and evaporating the solvents give crude title compound as a pale yellow oil.
후처리
- extractionextracted twice with EtOAc
- customThe solvent is evaporated
- washwashed twice with dichloromethane
- additionThe aqueous layer is adjusted to pH 9 by the addition of ammonium hydroxide solution
- extractionextracted with dichloromethane
- dry with materialDrying the combined organic layers over Na2SO4
- customevaporating the solvents
출처 및 근거
- ORD 기록
- ord-e6c65e702b144d18988ae03d0198767e
- 출처 데이터셋
- uspto-grants-2011_03
- 특허 번호
- US07897788B2
연결된 노트
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