Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341675생성일: 2026년 10월 26일
Hydrochloric Acid → 6-(3,5-Dimethylbiphenyl-4-yl)-2,2,4,4-tetramethylcyclohexane-1,3,5-trione
https://huagongshe.com/reaction/341675
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | Chloroform | HCID 6212 | — |
| 반응물 | 3,5-Dioxohexanoic acid | HCID 5459844 | — |
| 반응물 | 2,2,4,4-Tetramethylcyclohexane-1,3,5-trione | HCID 11769166 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 생성물 | 6-(3,5-Dimethylbiphenyl-4-yl)-2,2,4,4-tetramethylcyclohexane-1,3,5-trione | HCID 68732214 | — |
반응 단계
To a mixture of 2,2,4,4-tetramethylcyclohexane-1,3,5-trione (182 mg, 1 mmol) and 4-dimethylaminopyridine (610 mg, 5 mmol) under an atmosphere of nitrogen, is added dry chloroform (5.6 ml), followed by stirring at room temperature until dissolution is complete. To this solution is then added dry toluene (2 ml), and 3,5-dimethylbiphenylead triacetate (0.5 M solution in dry chloroform, 2.4 ml, 1.2 mmol). This solution is then heated under reflux for 1 hour. The reaction mixture is cooled to room temperature, acidified to pH 1 with 2N aqueous hydrochloric acid, filtered and the filtrate is extracted with dichloromethane (2×40 ml). The organic extracts are combined, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is further purified by column chromatography on silica gel to give 6-(3,5-dimethylbiphenyl-4-yl)-2,2,4,4-tetramethylcyclohexane-1,3,5-trione (166 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08895761B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_11 |
|---|
| ORD ID | ord-bca18a6890a54f3aab0a2c733f23c31a |
|---|
| 출처 메모 | uspto-grants-2014_11 |
|---|