Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1,1,1-Trichloroethane → 4-Chlorophenyl-2-[2-(1,2,4-triazol-1-yl)-prop-2-yl]-oxirane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1,1,1-Trichloroethane | HCID 6278 | — |
| 반응물 | Tetradecyltrimethylammonium | HCID 14251 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| 반응물 | 4-Chlorophenyl 2-(1,2,4-triazol-1-yl)-prop-2-yl ketone | HCID 13366855 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-Chlorophenyl-2-[2-(1,2,4-triazol-1-yl)-prop-2-yl]-oxirane | HCID 13366863 | 79% |
반응 단계
A mixture of 4'-chloro-2-methyl-2-(1H-1,2,4-triazol-1-yl)propiophenone (1.375 g), trimethyl sulphoxonium iodide (1.6 g), aqueous sodium hydroxide (5N; 13.5 ml.), cetrimide (80 mg.) and 1,1,1-trichloroethane (30 ml.) was heated at 80° for 24 hours. The solution was cooled and diluted with methylene chloride (30 ml.), and the organic layer was separated and dried (MgSO4). Removal of the solvent, followed by flash chromatography of the residue on silica (100 g.) using ethyl acetate/hexane/diethylamine (40:60:3 v/v/v) for elution, gave, after collection of appropriate fractions and evaporation, the title oxirane as an oil in 79% yield, 1.15 g.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04992454 |
| 출처 데이터셋 | uspto-grants-1991_02 |
| ORD ID | ord-d0ae63a853904f7ca0bc3f4b8bc88a2f |
| 출처 메모 | uspto-grants-1991_02 |