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Sodium borohydride → 4-Amino-3,5-dimethyl-alpha-[(methylsulfonyl)-methyl]-benzyl alcohol

HRID 542981
ノート
印刷プレビュー

反応式

HRID 542981 の反応式
[NH2:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([C:9](=[O:15])[CH2:10][S:11]([CH3:14])(=[O:13])=[O:12])=[CH:4][C:3]=1[CH3:16].[BH4-].[Na+]>>[NH2:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([CH:9]([OH:15])[CH2:10][S:11]([CH3:14])(=[O:13])=[O:12])=[CH:4][C:3]=1[CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 4311764Sodium borohydrideHCID 212810124'-Amino-3',5'-dimethyl-2-(methylsulfonyl)-acetophenone

生成物 1

HCID 538208514-Amino-3,5-dimethyl-alpha-[(methylsulfonyl)-methyl]-benzyl alcohol

実験手順

A suspension of 16.5 g. of 4'-amino-3',5'-dimethyl-2-(methylsulfonyl)-acetophenone and 10.6 g. of sodium borohydride in 500 ml. of alcohol was stirred at room temperature for 20 hours, resulting in a solution. After the addition of 500 ml. of water, the alcohol was evaporated under vacuum and the mixture was extracted with two 1 liter portions of ethyl acetate. The ethyl acetate extract was washed with two 500 ml. portions of water, dried over magnesium sulfate and evaporated under vacuum. After crystallization of the residue from ether, there was obtained 4-amino-3,5-dimethyl-α-[(methylsulfonyl)-methyl]-benzyl alcohol having a melting point of 146°-148° C.

後処理

  1. additionA suspension of 16.5 g
  • customresulting in a solution
  • additionAfter the addition of 500 ml
  • customof water, the alcohol was evaporated under vacuum
  • extractionthe mixture was extracted with two 1 liter portions of ethyl acetate
  • extractionThe ethyl acetate extract
  • washwas washed with two 500 ml
  • dry with materialportions of water, dried over magnesium sulfate
  • customevaporated under vacuum
  • customAfter crystallization of the residue from ether
  • 出典と根拠

    ORDレコード
    ord-3f669924b7b14177bdcc501eb3f61eeb
    出典データセット
    uspto-grants-1987_04
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04659818

    反応ノート

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