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Benzaldehyde → N-Benzyl-L-alaninol

HRID 1374978
ノート
印刷プレビュー

反応式

HRID 1374978 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 240BenzaldehydeHCID 80307L-AlaninolHCID 5049666Sodium triacetoxyborohydride

生成物 1

HCID 5356540N-Benzyl-L-alaninol

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 6344Dichloromethane溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-5428652c359045119c3877e3b9967944
出典データセット
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07166598B2

反応ノート

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