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4-chloro-N-methoxy-N-methyl-3-(methylsulfonyl)benzamide → 1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanone

HRID 1845143
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HRID 1845143 반응식
[Cl:1][C:2]1[CH:13]=[CH:12][C:5]([C:6](N(OC)C)=[O:7])=[CH:4][C:3]=1[S:14]([CH3:17])(=[O:16])=[O:15].[CH3:18][Mg]Br>O1CCCC1>[Cl:1][C:2]1[CH:13]=[CH:12][C:5]([C:6](=[O:7])[CH3:18])=[CH:4][C:3]=1[S:14]([CH3:17])(=[O:16])=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 581073914-chloro-N-methoxy-N-methyl-3-(methylsulfonyl)benzamideHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 581882281-(4-Chloro-3-(methylsulfonyl)phenyl)ethanone

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A round bottom flask was charged with 4-chloro-N-methoxy-N-methyl-3-(methylsulfonyl)benzamide (18.0 g, 64.9 mmol) and tetrahydrofuran (200 mL) at 0° C. Methylmagnesiumbromide (1M solution in THF, 78 mL, 78 mmol) was added slowly and the reaction was stirred for 3 h at that temperature. The reaction was then quenched with aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layers were concentrated under reduced pressure and the residue was purified by flash chromatography to get the title compound.

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후처리

  1. customThe reaction was then quenched with aqueous ammonium chloride solution
  2. extractionextracted with ethyl acetate
  3. concentrationThe organic layers were concentrated under reduced pressure
  4. customthe residue was purified by flash chromatography

출처 및 근거

ORD 기록
ord-e187ae654982486094a513dcbf0ac83c
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08946439B2

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