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2-Bromobutanoyl chloride → 2-Bromo-1-(5-chlorobenzo[b]thiophen-2-yl)butan-1-one

HRID 2183619
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HRID 2183619 반응식
[Br:1][CH:2]([CH2:6][CH3:7])[C:3](Cl)=[O:4].[Cl-].[Al+3].[Cl-].[Cl-].[Cl:12][C:13]1[CH:21]=[CH:20][C:16]2[S:17][CH:18]=[CH:19][C:15]=2[CH:14]=1>ClCCl>[Br:1][CH:2]([CH2:6][CH3:7])[C:3]([C:18]1[S:17][C:16]2[CH:20]=[CH:21][C:13]([Cl:12])=[CH:14][C:15]=2[CH:19]=1)=[O:4]
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참가 물질

5

반응물 3

HCID 907342-Bromobutanoyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 113097545-Chlorobenzo(b)thiophene

생성물 1

HCID 224740212-Bromo-1-(5-chlorobenzo[b]thiophen-2-yl)butan-1-one

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

A solution of 2-bromobutyryl chloride (8 g) in dichloromethane (15 ml) was added dropwise under nitrogen at ambient temperature to a stirred suspension of anhydrous aluminium chloride (12 g) in dichloromethane (100 ml). When the addition was complete, a solution of 5-chlorobenzo[b]thiophene (5 g; prepared in a manner similar to that described in J. Heterocyclic Chem., 1988, 25, 1271) in dichloromethane (30 ml) was added dropwise, then the mixture was stirred at ambient temperature for 1 hour and added to ice-cold water (500 ml). The mixture was stirred at ambient temperature for 30 minutes then the product was extracted into dichloromethane (100 ml). The extract was washed with water (2×30 ml) and saturated aqueous sodium chloride solution (2×30 ml), then it was dried (Na2SO4) and the solvent was removed in vacuo. The residue was purified by repeated (5-fold) flash chromatography over silica using a 19:1 mixture of petroleum ether (b.p. 60-80° C.) and ethyl acetate as eluant. Appropriate fractions were combined and the solvents removed in vacuo to give 2-bromo-1-(5-chlorobenzo[b]thiophen-2-yl)butan-1-one (1.04 g) as an off-white solid which was used without further purification.

후처리

  1. additionWhen the addition
  2. customprepared in a manner similar to
  3. stirringThe mixture was stirred at ambient temperature for 30 minutes
  4. extractionthe product was extracted into dichloromethane (100 ml)
  5. washThe extract was washed with water (2×30 ml) and saturated aqueous sodium chloride solution (2×30 ml)
  6. dry with materialit was dried (Na2SO4)
  7. customthe solvent was removed in vacuo
  8. customThe residue was purified
  9. additiona 19:1 mixture of petroleum ether (b.p. 60-80° C.) and ethyl acetate as eluant
  10. customthe solvents removed in vacuo

출처 및 근거

ORD 기록
ord-d77f16ad07264c6b992c6e4b5b4f6095
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06900216B2

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