Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930106Generated: October 31, 2026

Methanol → Methyl 2-(2-chloro-2',6'-difluoro-4'-hydroxybiphenyl-4-yl)acetate

https://huagongshe.com/reaction/1930106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
Reactant2-(2-Chloro-2',6'-difluoro-4'-methoxybiphenyl-4-yl)acetic acidHCID 59627715—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(2-chloro-2',6'-difluoro-4'-hydroxybiphenyl-4-yl)acetateHCID 59627694100%

Reaction Steps

Boron tribromide (1.494 mL, 15.80 mmol) was added dropwise to 2-(2-chloro-2′,6′-difluoro-4′-methoxybiphenyl-4-yl)acetic acid (Intermediate 2-5; 822 mg, 2.63 mmol) in dichloromethane (30 mL) at ambient temperature under nitrogen. The resulting solution was stirred at ambient temperature for 90 minutes. The reaction mixture was cautiously added to ice water cooled methanol (50 mL) and the mixture was stirred for a further 20 minutes. The reaction mixture was evaporated to dryness and redissolved in EtOAc (150 mL), and washed sequentially with 2M HCl (50 mL) and saturated brine (50 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford methyl 2-(2-chloro-2′,6′-difluoro-4′-hydroxybiphenyl-4-yl)acetate (822 mg, 100%) as a yellow gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188092B2
Source datasetuspto-grants-2012_05
ORD IDord-aa3013bcf67543ef97e805665623c991
Source noteuspto-grants-2012_05