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Methyl 4-(hydroxymethyl)-2-(trifluoromethyl)benzoate → Methyl 4-formyl-2-(trifluoromethyl)benzoate

HRID 467936
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HRID 467936 반응식
[CH3:1][O:2][C:3](=[O:16])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][OH:11])=[CH:6][C:5]=1[C:12]([F:15])([F:14])[F:13]>ClCCl.[O-2].[O-2].[Mn+4]>[CH3:1][O:2][C:3](=[O:16])[C:4]1[CH:9]=[CH:8][C:7]([CH:10]=[O:11])=[CH:6][C:5]=1[C:12]([F:13])([F:15])[F:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 57443316Methyl 4-(hydroxymethyl)-2-(trifluoromethyl)benzoate

생성물 1

HCID 57443312Methyl 4-formyl-2-(trifluoromethyl)benzoate수율 84.4%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 6344Dichloromethane용매

실험 절차

To a solution of 4-hydroxymethyl-2-trifluoromethyl-benzoic acid methyl ester (Example I9) (7.15 g) in dichloromethane (150 ml) was added manganese dioxide (25.1 g). The reaction mixture stirred at ambient temperature for 2.5 hours. The reaction mixture was filtered over a plug of silica gel and the filtrate concentrated to give 4-formyl-2-trifluoromethyl-benzoic acid methyl ester (5.98 g), which was used without further purification. 1H-NMR (CDCl3, 400 MHz): 10.11 (s, 1H), 8.25-7.59 (m, 3H), 3.98 (s, 3H).

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후처리

  1. filtrationThe reaction mixture was filtered over a plug of silica gel
  2. concentrationthe filtrate concentrated

출처 및 근거

ORD 기록
ord-a733c875d2bf48a18fcee5c33c163168
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08623896B2

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