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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Pentamethyldiethylenetriamine | HCID 18196 | — |
| 반응물 | Ethyl oxoacetate | HCID 70211 | — |
| 반응물 | Tert-butyl-(2,4-difluoro-phenoxy)-diphenyl-silane | HCID 21904942 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Hexane | HCID 8058 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 생성물 | (RS)-[3-(tert-butyl-diphenyl-silanyloxy)-2,6-difluoro-phenyl]-hydroxy-acetic acid ethyl ester | HCID 69290212 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07129238B2 |
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| 출처 데이터셋 | uspto-grants-2006_10 |
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| ORD ID | ord-c19e0c27070343f4967fb8f61c10d3c2 |
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| 출처 메모 | uspto-grants-2006_10 |
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