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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270152생성일: 2026년 10월 25일

1,2-Dichloroethane → Ethyl 4-({[tert-butyl(diphenyl)silyl]oxy}methyl)-2-(4-{trifluoromethyl}phenyl)-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/270152

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물WaterHCID 962—
반응물4-(Trifluoromethyl)thiobenzamideHCID 2734823—
반응물Ethyl 4-{[tert-butyl(diphenyl)silyl]oxy}2-chloro-3-oxobutanoateHCID 17951839—
용매DichloromethaneHCID 6344—
생성물Ethyl 4-({[tert-butyl(diphenyl)silyl]oxy}methyl)-2-(4-{trifluoromethyl}phenyl)-1,3-thiazole-5-carboxylateHCID 1795180076%

반응 단계

To a 500ml round-bottom flask equipped with a magnetic stir-bar was mixed ethyl 4-{[tert-butyl(diphenyl)silyl]oxy}-2-chloro-3-oxobutanoate (20.4g, 52.88mmoles, 1eq), 4-trifluoromethylthiobenzamide (12.2g, 59.5mmoles, 1.1eq), 1,2-dichloroethane (150ml, 0.44M) and H2O (3ml). This mixture was refluxed for 12hrs. After cooling to room temperature, the reaction mixture was diluted with CH2Cl2(100ml) and washed with sat. NaHCO3. Once the phases were separated, the organic phase washed with water, brine and dried over Na2SO4. This was then filtered, concentrated in vacuo and purified via silica gel chromatography (5% EtOAc/Hexanes to 20% EtOAc/Hexanes) to yield 20.3g (76%) of the titled compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449468B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-c69fbdd2ad324f929bc0c46723c1d169
출처 메모uspto-grants-2008_11