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

HRID 974374
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HRID 974374 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

HCID 199863443-Bromo-7-benzothiophene-carbaldehyde

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-1ae22274ec364f248ee7d34599f174ce
출처 데이터셋
uspto-grants-1991_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05068359

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