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HRID 129589作成日:2026年10月26日

Methanol → Methyl 2-(3-hydroxyphenoxy)phenylacetate

https://huagongshe.com/reaction/129589

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Boron tribromideHCID 25134—
反応物Sodium BicarbonateHCID 516892—
反応物Methyl 2-(3-methoxyphenoxy)phenylacetateHCID 14620154—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Methyl 2-(3-hydroxyphenoxy)phenylacetateHCID 1462015592.3%

反応条件

温度2.5 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05468857
出典データセットuspto-grants-1995_11
ORD IDord-46dcf072d19d41bba9b1e40f880a09d3
出典メモuspto-grants-1995_11