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Benzaldehyde → N-Benzyl-L-alaninol

HRID 1374978
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HRID 1374978 반응식
C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[NH2:15][C@@H:16]([CH3:19])[CH2:17][OH:18].[CH:20](=O)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>ClCCl.C(O)(=O)C>[CH2:20]([NH:15][C@@H:16]([CH3:19])[CH2:17][OH:18])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 240BenzaldehydeHCID 80307L-AlaninolHCID 5049666Sodium triacetoxyborohydride

생성물 1

HCID 5356540N-Benzyl-L-alaninol

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 6344Dichloromethane용매

실험 절차

Sodium triacetoxyborohydride (36.7 g) was added portion wisely to a mixture of (2S)-2-amino-1-propanol (10.0 g) and benzaldehyde (13.53 ml) in a mixture of dichloromethane (140 ml) and acetic acid (8.38 ml) at 0° C. and the whole was stirred at room temperature overnight. The mixture was washed successively with 2N sodium hydroxide and brine, and dried over sodium sulfate. The solution was evaporated under reduced pressure and the resulting residue was purified by column chromatography on silica gel using a mixed solvent of dichloromethane and methanol (30:1). The fractions containing the objective compound were collected and evaporated under reduced pressure to give (2S)-2-benzylamino-1-propanol (15.96 g).

후처리

  1. washThe mixture was washed successively with 2N sodium hydroxide and brine
  2. dry with materialdried over sodium sulfate
  3. customThe solution was evaporated under reduced pressure
  4. customthe resulting residue was purified by column chromatography on silica gel using a mixed solvent of dichloromethane and methanol (30:1)
  5. additionThe fractions containing the objective compound
  6. customwere collected
  7. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-5428652c359045119c3877e3b9967944
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07166598B2

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