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3,3,3-trifluoro-N-(2-(hydroxymethyl)-4-methoxyphenyl)propanamide → 3,3,3-trifluoro-N-(2-formyl-4-methoxyphenyl)propanamide

HRID 1472713
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인쇄 미리보기

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HRID 1472713 반응식
[F:1][C:2]([F:18])([F:17])[CH2:3][C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][C:8]=1[CH2:15][OH:16])=[O:5]>C(Cl)Cl.O=[Mn]=O>[F:1][C:2]([F:17])([F:18])[CH2:3][C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][C:8]=1[CH:15]=[O:16])=[O:5]
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참가 물질

4

반응물 1

HCID 669800523,3,3-trifluoro-N-(2-(hydroxymethyl)-4-methoxyphenyl)propanamide

생성물 1

HCID 866899383,3,3-trifluoro-N-(2-formyl-4-methoxyphenyl)propanamide수율 84.9%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 6344Dichloromethane용매

실험 절차

To a solution of 3,3,3-trifluoro-N-(2-(hydroxymethyl)-4-methoxyphenyl)propanamide (6.30 g, 23.9 mmol) in anhydrous CH2Cl2 (200 mL) was added MnO2 (20.0 g, 229 mmol). The mixture was refluxed for 16 hours. The mixture was filtered off and the filtrate was concentrated to give the product (5.30 g, yield 84%).

후처리

  1. temperatureThe mixture was refluxed for 16 hours
  2. filtrationThe mixture was filtered off
  3. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-0fd669e54bde429c972c1a1e1ea52d5a
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09012646B2

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