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Sodium amide → 4-Amino-3,5-dimethylbenzaldehyde

HRID 462557
ノート
印刷プレビュー

反応式

HRID 462557 の反応式
[NH2:1][C:2]1[C:14]([CH3:15])=[CH:13][C:5]([CH:6]([OH:12])CS(C)(=O)=O)=[CH:4][C:3]=1[CH3:16].[NH2-].[Na+]>CS(C)=O>[NH2:1][C:2]1[C:3]([CH3:16])=[CH:4][C:5]([CH:6]=[O:12])=[CH:13][C:14]=1[CH3:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24533Sodium amideHCID 538208514-Amino-3,5-dimethyl-alpha-[(methylsulfonyl)-methyl]-benzyl alcohol

生成物 1

HCID 100347774-Amino-3,5-dimethylbenzaldehyde

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

A solution of 14.6 g. of 4-amino-3,5-dimethyl-α-[(methylsulfonyl)-methyl]-benzyl alcohol in 50 ml. of absolute dimethylsulfoxide was treated with 1.17 g. of sodium amide, stirred for 2 hours at room temperature, diluted with 500 ml. of water and extracted with two 500 ml. portions of ethyl acetate. The ethyl acetate extract was washed with two 200 ml. portions of water and evaporated under vacuum. After recrystallization of the residue from cyclohexane, there was obtained 4-amino-3,5-dimethyl-benzaldehyde having a melting point of 75°-76° C.

後処理

  1. additiondiluted with 500 ml
  2. extractionof water and extracted with two 500 ml
  3. extractionThe ethyl acetate extract
  4. washwas washed with two 200 ml
  5. customportions of water and evaporated under vacuum
  6. customAfter recrystallization of the residue from cyclohexane

出典と根拠

ORDレコード
ord-108e6ab545a343b5b07e1a58cbf918c3
出典データセット
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04515948

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート