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Azobisisobutyronitrile → Methyl 4-(bromomethyl)-3-chlorothiophene-2-carboxylate

HRID 901944
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인쇄 미리보기

반응식

HRID 901944 반응식
[Cl:1][C:2]1[C:6]([CH3:7])=[CH:5][S:4][C:3]=1[C:8]([O:10][CH3:11])=[O:9].[Br:12]N1C(=O)CCC1=O.N(C(C)(C)C#N)=NC(C)(C)C#N>C(Cl)(Cl)(Cl)Cl>[Br:12][CH2:7][C:6]1[C:2]([Cl:1])=[C:3]([C:8]([O:10][CH3:11])=[O:9])[S:4][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6547AzobisisobutyronitrileHCID 67184N-bromobutanimideHCID 2777567Methyl 3-chloro-4-methylthiophene-2-carboxylate

생성물 1

HCID 18376575Methyl 4-(bromomethyl)-3-chlorothiophene-2-carboxylate수율 39%

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

A solution of methyl 3-chloro-4-methylthiophenecarboxylate (10 g, 53 mmol), N-bromosuccinimide (9.4 g, 53 mmol) and azo-bis-(isobutyronitrile) (860 mg, 5.3 mmol) in carbon tetrachloride (300 ml) was heated at reflux for 18 h. The mixture was filtered and reduced. Chromatography (10% EtOAc/90% hexanes) afforded methyl 4-bromomethyl-3-chlorothiophene-2-carboxylate (5.5 g, 39%) as a white solid.

후처리

  1. temperatureat reflux for 18 h
  2. filtrationThe mixture was filtered

출처 및 근거

ORD 기록
ord-c153adddf8964eab96439cd0dfd244d4
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07365065B2

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