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Hydrochloric Acid → 1-(4-Chlorobenzo[b]thiophen-2-yl)butan-1-one

HRID 2183643
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HRID 2183643 반응식
[CH2:1]([Mg]Cl)[CH2:2][CH3:3].[Cl:6][C:7]1[C:15]2[CH:14]=[C:13]([C:16](N(OC)C)=[O:17])[S:12][C:11]=2[CH:10]=[CH:9][CH:8]=1.O.Cl>O1CCCC1>[Cl:6][C:7]1[C:15]2[CH:14]=[C:13]([C:16](=[O:17])[CH2:1][CH2:2][CH3:3])[S:12][C:11]=2[CH:10]=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 224738924-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamideHCID 178455855HCID 178455855, 화합물2회

생성물 1

HCID 224736901-(4-Chlorobenzo[b]thiophen-2-yl)butan-1-one

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매

실험 절차

Propylmagnesium chloride (2M solution in ether; 4.3 ml) was added under nitrogen over 15 minutes to a stirred solution of 4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamide (2 g) in tetrahydrofuran (25 ml) then the mixture was stirred at ambient temperature for 2.33 hours. Further propylmagnesium chloride (2M solution in ether; 0.5 ml) was added, the mixture was stirred at ambient temperature for 0.5 hours, then water (150 ml) and 5M hydrochloric acid (15 ml) were added. The product was extracted into dichloromethane (3×40 ml), the combined extracts were dried (MgSO4) and the solvents were removed in vacuo. The residue was purified by column chromatography over silica using dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to leave 1-(4-chlorobenzo[b]thiophen-2-yl)butan-1-one (0.95 g) which was used without further purification.

후처리

  1. stirringthe mixture was stirred at ambient temperature for 0.5 hours
  2. extractionThe product was extracted into dichloromethane (3×40 ml)
  3. dry with materialthe combined extracts were dried (MgSO4)
  4. customthe solvents were removed in vacuo
  5. customThe residue was purified by column chromatography over silica
  6. customthe solvents removed in vacuo

출처 및 근거

ORD 기록
ord-5cc97c0fdbce4ef689ec890feda21870
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06900216B2

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