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

HRID 1474724
Notes
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Reaction equation

HRID 1474724 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 6344Dichloromethane2×HCID 25134Boron tribromideHCID 51873792-(2,6-Difluoro-4-methoxyphenyl)acetic acid

Product 1

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

Procedure

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).

Workup

  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)

Sources & evidence

ORD record
ord-b9a8b9c3000b42259b648604ce95a09a
Source dataset
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09018224B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes