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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741869Generated: October 25, 2026

Methanol → Methyl 2-(3-hydroxyphenoxy)phenylacetate

https://huagongshe.com/reaction/1741869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 2-(3-methoxyphenoxy)phenylacetateHCID 14620154—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(3-hydroxyphenoxy)phenylacetateHCID 1462015592.3%

Reaction Steps

Boron tribromide (12.89 g, 0.051 mol) was dissolved in dichloromethane (50 ml) and cooled to 0°-5° C. A solution of methyl 2-(3-methoxyphenoxy)phenylacetate (7.0 g; 0,026 mol) in dichloromethane (80 ml) was added dropwise, with stirring over 1 hour. After stirring at 0°-5° C. for 20 minutes the mixture was added dropwise, with stirring to absolute methanol (100 ml) maintaining the temperature at 0°-5° C. The resulting solution was poured into water (250 ml) containing sodium bicarbonate (12 g), and the resulting mixture was extracted with ether (500 mls). The organic phase was washed with water (3×200 ml) and saturated brine (150 ml). After drying and filtration, evaporation of the ether solution gave methyl 2-(3-hydroxyphenoxy)phenylacetate (D) (6.12 g, 92.3% yield) as a brown gum. This material was suitable for use in subsequent steps without further purification. However, chromatography using mixtures of ether and hexane as eluant gave material of higher purity as a viscous golden oil which rapidly darkened on exposure to air.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05334748
Source datasetuspto-grants-1994_08
ORD IDord-1d6383ec4a74413994147ad4017d3b84
Source noteuspto-grants-1994_08