돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1247381생성일: 2026년 10월 26일

Water → (RS)-(2,6-difluoro-3-hydroxy-phenyl)-ethoxy-acetic acid

https://huagongshe.com/reaction/1247381

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물(RS)-[3-(tert-butyl-diphenyl-silanyloxy)-2,6-difluoro-phenyl]-ethoxy-acetic acid ethyl esterHCID 69290209—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물(RS)-(2,6-difluoro-3-hydroxy-phenyl)-ethoxy-acetic acidHCID 2190541699%

반응 조건

온도65 °C

반응 단계

To a solution of (RS)-[3-(tert-butyl-diphenyl-silanyloxy)-2,6-difluoro-phenyl]-ethoxy-acetic acid ethyl ester (62.5 g) in THF (250 ml) and MeOH (250 ml) was added H2O (200 ml) and LiOH.H2O (10.5 g) and it was stirred 2 h at 65° C. MeOH and THF were evaporated and the aqueous residue was washed with Hept/Et2O 9:1 (2×150 ml). The organic layers were extracted with two portions of H2O (200 ml). The combined aqueous layers were cooled in an ice bath and acidified with 35 ml 25% aq. HCl. Extraction with AcOEt (3×200 ml) followed by washing with brine, drying (Na2SO4) and evaporation of the solvent afforded 28.7 g (99%) of (RS)-(2,6-difluoro-3-hydroxy-phenyl)-ethoxy-acetic acid. Yellow viscous oil. MS 231.2 ([M−H]−).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07129238B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-b5fe155d56594b88ba2bffe8f3974b7d
출처 메모uspto-grants-2006_10