Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
tert-Butyl hydroperoxide → 2,3-Difluoro-4-octyloxyphenyl 4-hexyloxybenzoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | tert-Butyl hydroperoxide | HCID 6410 | — |
| 반응물 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 반응물 | 2-Dimethylaminopyridine | HCID 21885 | — |
| 반응물 | 4-(Hexyloxy)benzoic acid | HCID 70834 | — |
| 반응물 | 2,3-Difluoro-4octyloxyphenol | HCID 14766703 | — |
| 반응물 | 2,3-Difluorooctyloxybenzene | HCID 19103632 | — |
| 반응물 | CID 86747250 | HCID 86747250 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2,3-Difluoro-4-octyloxyphenyl 4-hexyloxybenzoate | HCID 19103718 | — |
반응 단계
0.1 mol of 4-hexyloxybenzoic acid, 0.01 mol of dimethylaminopyridine and 0.1 mol of 2,3-difluoro-4octyloxyphenol (preparable from 2,3-difluorooctyloxybenzene by lithiation at -70° to -80° and dropwise addition of a solution of lithium t-butylperoxide in ether prepared from 0.12 mol of t-butyl hydroperoxide and 0.12 mol of butyllithium) are introduced into 150 ml of dichloromethane, a solution of 0.1 mol of dicyclohexylcarbodiimide in 30 ml of dichloromethane is added dropwise with stirring at 10o, and the mixture is subsequently stirred at room temperature for 15 hours. The mixture is filtered through silica gel, the solvent is evaporated, and 2,3-difluoro-4-octyloxyphenyl 4-hexyloxybenzoate is obtained as the residue.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05248447 |
| 출처 데이터셋 | uspto-grants-1993_09 |
| ORD ID | ord-82e83c02b9134508a72b2b79ba90c519 |
| 출처 메모 | uspto-grants-1993_09 |