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Methanol → 2-Fluoro-5-methoxy-4-nitrobenzoic acid

HRID 1880855
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HRID 1880855 반응식
C[O:2][C:3](=[O:15])[C:4]1[CH:9]=[C:8](F)[C:7]([N+:11]([O-:13])=[O:12])=[CH:6][C:5]=1[F:14].[OH-:16].[K+].[CH3:18]O>>[F:14][C:5]1[CH:6]=[C:7]([N+:11]([O-:13])=[O:12])[C:8]([O:16][CH3:18])=[CH:9][C:4]=1[C:3]([OH:2])=[O:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 14797Potassium HydroxideHCID 18526058Methyl 2,5-difluoro-4-nitrobenzoate

생성물 1

HCID 579556142-Fluoro-5-methoxy-4-nitrobenzoic acid

반응 조건

온도
80 °C

실험 절차

To a solution of methyl-2,5-difluoro-4-nitrobenzoate (10 g, 46 mmol) in methanol (100 mL) was added potassium hydroxide (7.73 g, 184 mmol) in two batches. The reaction mixture was stirred in an oil bath at 80° C. for 1 h. It was then concentrated, acidified with HCl. Solid was filtered, washed with water and dried to give the product as light yellow powder (10 g, quantitative yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 3.95 (s, 3 H) 7.66 (d, J=4 Hz, 1 H) 8.01 (d, J=8 Hz, 1 H). [M+H] calc'd for C8H6FNO5, 216; found 216.

후처리

  1. concentrationIt was then concentrated
  2. filtrationSolid was filtered
  3. washwashed with water
  4. customdried

출처 및 근거

ORD 기록
ord-5e9bc02c459e403281b7756ed5fefa57
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318727B2

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