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Chlorosuccinimide → 5-Chloro-N-methoxy-N-methyl-3-thiophenecarboxamide

HRID 626106
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HRID 626106 반응식
[CH3:1][O:2][N:3]([CH3:11])[C:4]([C:6]1[CH:10]=[CH:9][S:8][CH:7]=1)=[O:5].[Cl:12]N1C(=O)CCC1=O>CC(O)=O>[Cl:12][C:9]1[S:8][CH:7]=[C:6]([C:4]([N:3]([O:2][CH3:1])[CH3:11])=[O:5])[CH:10]=1
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참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 22489894N-methoxy-N-methylthiophene-3-carboxamide

생성물 1

HCID 876931115-Chloro-N-methoxy-N-methyl-3-thiophenecarboxamide수율 50.2%

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
120 °C

실험 절차

To a stirred solution of N-methoxy-N-methylthiophene-3-carboxamide (5.0 g, 1.0 eq, prepared from Example 12 step A) in 50 mL CH3COOH was added N-chlorosuccinimide (3.88 g, 1.0 eq). The mixture was then reflux at 120° C. for 4 h. After quenching with water, the mixture was extracted with ethyl acetate. The extract was washed with brine, dried, concentrated, and purified by column chromatography to get 3.0 g desired product (40% yield).

후처리

  1. customAfter quenching with water
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe extract was washed with brine
  4. customdried
  5. concentrationconcentrated
  6. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-a4771230c0664c0080f603dfa08806ab
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09309211B2

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