Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1,2-Dichloroethane → Ethyl 4-({[tert-butyl(diphenyl)silyl]oxy}methyl)-2-(4-{trifluoromethyl}phenyl)-1,3-thiazole-5-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1,2-Dichloroethane | HCID 11 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | 4-(Trifluoromethyl)thiobenzamide | HCID 2734823 | — |
| 반응물 | Ethyl 4-{[tert-butyl(diphenyl)silyl]oxy}2-chloro-3-oxobutanoate | HCID 17951839 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Ethyl 4-({[tert-butyl(diphenyl)silyl]oxy}methyl)-2-(4-{trifluoromethyl}phenyl)-1,3-thiazole-5-carboxylate | HCID 17951800 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07449468B2 |
| 출처 데이터셋 | uspto-grants-2008_11 |
| ORD ID | ord-c69fbdd2ad324f929bc0c46723c1d169 |
| 출처 메모 | uspto-grants-2008_11 |