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2-Nitropropane → 3-Bromo-7-benzothiophene-carbaldehyde

HRID 974374
ノート
印刷プレビュー

反応式

HRID 974374 の反応式
[N+](C(C)C)([O-])=[O:2].[Na].[Br:8][C:9]1[C:13]2[CH:14]=[CH:15][CH:16]=[C:17]([CH2:18]Br)[C:12]=2[S:11][CH:10]=1>C(O)C>[Br:8][C:9]1[C:13]2[CH:14]=[CH:15][CH:16]=[C:17]([CH:18]=[O:2])[C:12]=2[S:11][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3982-NitropropaneHCID 5360545SodiumHCID 147805223-Bromo-7-bromomethylbenzothiophene

生成物 1

HCID 199863443-Bromo-7-benzothiophene-carbaldehyde

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

With stirring, 68.2 g (0.74 mole) of 2-nitropropane are added dropwise at room temperature, over a period of 45 minutes, to a Na-ethoxide solution prepared under an argon atmosphere from 14.2 g (0.61 mole) of sodium and 800 ml of abs. ethanol. 137 g (0.61 mole) of 3-bromo-7-bromomethylbenzothiophene are then added dropwise at room temperature, over a period of 1.5 hours, to the resulting white suspension. After the reaction mixture has been stirred for one day, the solvent is evaporated off from the reaction mixture in vacuo, the resulting residue of 101.2 g is dissolved in a mixture of hexane:diethyl ether 1:1 and the solution is purified by chromatography on silica gel. After evaporation of the solvent, 81 g (80% of the theoretical amount) of 3-bromo-7-benzothiophene-carbaldehyde are obtained as residue.

後処理

  1. stirringAfter the reaction mixture has been stirred for one day
  2. customthe solvent is evaporated off from the reaction mixture in vacuo
  3. dissolutionthe resulting residue of 101.2 g is dissolved in a mixture of hexane:diethyl ether 1:1
  4. customthe solution is purified by chromatography on silica gel
  5. customAfter evaporation of the solvent, 81 g (80% of the theoretical amount) of 3-bromo-7-benzothiophene-carbaldehyde
  6. customare obtained as residue

出典と根拠

ORDレコード
ord-1ae22274ec364f248ee7d34599f174ce
出典データセット
uspto-grants-1991_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05068359

反応ノート

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