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Dichloromethane → Benzeneacetic acid, 2,6-difluoro-4-hydroxy-, methyl ester

HRID 1474724
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HRID 1474724 반응식
[F:1][C:2]1[CH:7]=[C:6]([O:8]C)[CH:5]=[C:4]([F:10])[C:3]=1[CH2:11][C:12]([OH:14])=[O:13].B(Br)(Br)Br.Cl[CH2:20]Cl>>[F:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[C:4]([F:10])[C:3]=1[CH2:11][C:12]([O:14][CH3:20])=[O:13]
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참가 물질

4

반응물 3

HCID 6344Dichloromethane2회HCID 25134Boron tribromideHCID 51873792-(2,6-Difluoro-4-methoxyphenyl)acetic acid

생성물 1

HCID 68228239Benzeneacetic acid, 2,6-difluoro-4-hydroxy-, methyl ester

실험 절차

To a stirred solution of (2,6-difluoro-4-methoxyphenyl)acetic acid (1.50 g, 7.42 mmol) in 20 ml anhydrous dichloromethane at 0° C. was added a solution of boron tribromide (4.29 ml, 44.5 mmol) in 10 ml anhydrous dichloromethane. The cooling bath was removed and the mixture allowed to warm to RT for 2 hours. The reaction was diluted with 20 ml anhydrous methanol, and stirred for 30 minutes. The mixture was concentrated under reduced pressure, and the residue purified by column chromatography on silica gel, (Biotage column, 50 g) using a gradient eluent of 0-30% ethyl acetate in hexanes (700 ml) to afford the title compound. 1H NMR (CDCl3): δ 6.30 (d, J=8.3 Hz, 2H), 6.12 (br, 1H), 3.76 (s, 3H), 3.63 (s, 2H).

후처리

  1. customThe cooling bath was removed
  2. additionThe reaction was diluted with 20 ml anhydrous methanol
  3. concentrationThe mixture was concentrated under reduced pressure
  4. customthe residue purified by column chromatography on silica gel, (Biotage column, 50 g)

출처 및 근거

ORD 기록
ord-b9a8b9c3000b42259b648604ce95a09a
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09018224B2

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