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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1247379생성일: 2026년 10월 27일

Hydrochloric Acid → (RS)-[3-(tert-butyl-diphenyl-silanyloxy)-2,6-difluoro-phenyl]-hydroxy-acetic acid ethyl ester

https://huagongshe.com/reaction/1247379

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PentamethyldiethylenetriamineHCID 18196—
반응물Ethyl oxoacetateHCID 70211—
반응물Tert-butyl-(2,4-difluoro-phenoxy)-diphenyl-silaneHCID 21904942—
반응물ButyllithiumHCID 178418339—
용매TolueneHCID 1140—
용매HexaneHCID 8058—
용매1,2-DimethoxyethaneHCID 8071—
생성물(RS)-[3-(tert-butyl-diphenyl-silanyloxy)-2,6-difluoro-phenyl]-hydroxy-acetic acid ethyl esterHCID 6929021254%

반응 조건

온도-70 °C

반응 단계

A solution under Ar of tert-butyl-(2,4-difluoro-phenoxy)-diphenyl-silane (102 g) and 1,1,4,7,7-pentamethyldiethylenetriamine (50.6 g) in DME (800 ml) was cooled to −70° C. before addition of 1.6 N n-BuLi in hexane (182 ml) over a period of 1 h. The yellow solution was stirred 1 h at −70° C. 50% glyoxalic acid ethylester in toluene (113 g) was added over a period of 1 h. The reaction mixture was stirred 2 h more at −70° C. before heating up over 1 h to 0° C. Sat. NH4 sol. (300 ml) was added and the pH was lowered to pH=6 with 2 N HCl. The product was extracted with AcOEt (2×400 ml). The organic layers were washed with brine (500 ml) and dried (Na2SO4) and the solvent was evaporated. CC (Hept to Hept/AcOEt 9:1) afforded 70.8 g (54%) of (RS)-[3-(tert-butyl-diphenyl-silanyloxy)-2,6-difluoro-phenyl]-hydroxy-acetic acid ethyl ester. Yellowish oil. MS 488.5 ([M+H]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07129238B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-c19e0c27070343f4967fb8f61c10d3c2
출처 메모uspto-grants-2006_10