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Methanol → N-(3-(4-Carbomethoxyphenyl)-1-methylpropyl)-2-hydroxy-2-(3-trifluoromethylphenyl)ethanamine

HRID 434376
ノート
印刷プレビュー

反応式

HRID 434376 の反応式
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][CH2:12][C:13](=O)[CH3:14])=[CH:7][CH:6]=1)([O:3][CH3:4])=[O:2].[OH:16][CH:17]([C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:28])[F:27])[CH:21]=1)[CH2:18][NH2:19].CO.[BH4-].[Na+]>C1C=CC=CC=1>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][CH2:12][CH:13]([NH:19][CH2:18][CH:17]([OH:16])[C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:28])([F:29])[F:27])[CH:21]=2)[CH3:14])=[CH:7][CH:6]=1)([O:3][CH3:4])=[O:2]
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 4

HCID 887MethanolHCID 305142-Amino-1-[3-(trifluoromethyl)phenyl]ethan-1-olHCID 4311764Sodium borohydrideHCID 109326404-(3-Oxobutyl)benzoic acid methyl ester

生成物 1

HCID 20493837N-(3-(4-Carbomethoxyphenyl)-1-methylpropyl)-2-hydroxy-2-(3-trifluoromethylphenyl)ethanamine

試薬・触媒・溶媒 1

HCID 241
Benzene
溶媒

実験手順

A mixture of 4-(4-carbomethoxyphenyl) butan-2-one (3.0 g) and 2-hydroxy-2-(3-trifluoromethylphenyl) ethanamine (3.0 g) in dry benzene (100 ml) was refluxed under Dean and Stark conditions for 2 hours. The solvent was replaced with methanol (100 ml) and sodium borohydride (2.0 g) was added portionwise with ice cooling. The mixture was stirred at ambient temperature for 2 hours, the solvent was evaporated and the residue was partitioned between water (100 ml) and chloroform (100 ml). The organic phase was dried (MgSO4) and evaporated to an oil, which was chromatographed on silica gel 60 in 3% methanol/chloroform. The title compound was obtained as a colourless oil.

後処理

  1. temperaturewas refluxed under Dean and Stark conditions for 2 hours
  2. additionwas added portionwise with ice cooling
  3. customthe solvent was evaporated
  4. customthe residue was partitioned between water (100 ml) and chloroform (100 ml)
  5. dry with materialThe organic phase was dried (MgSO4)
  6. customevaporated to an oil, which
  7. customwas chromatographed on silica gel 60 in 3% methanol/chloroform

出典と根拠

ORDレコード
ord-c31c22f76520487db83f593564262688
出典データセット
uspto-grants-1983_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04396627

反応ノート

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