돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129589생성일: 2026년 10월 25일

Methanol → Methyl 2-(3-hydroxyphenoxy)phenylacetate

https://huagongshe.com/reaction/129589

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Boron tribromideHCID 25134—
반응물Sodium BicarbonateHCID 516892—
반응물Methyl 2-(3-methoxyphenoxy)phenylacetateHCID 14620154—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Methyl 2-(3-hydroxyphenoxy)phenylacetateHCID 1462015592.3%

반응 조건

온도2.5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05468857
출처 데이터셋uspto-grants-1995_11
ORD IDord-46dcf072d19d41bba9b1e40f880a09d3
출처 메모uspto-grants-1995_11