Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Potassium Hydroxide → alpha-Cyclohexylthiomethyl-beta-(p-methoxyphenyl)-gamma-butyrolactone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Cyclohexanethiol | HCID 15290 | — |
| 반응물 | alpha-Methanesulfonyloxymethyl-beta-(p-methoxyphenyl)-gamma-butyrolactone | HCID 20234197 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | alpha-Cyclohexylthiomethyl-beta-(p-methoxyphenyl)-gamma-butyrolactone | HCID 13518978 | 22% |
반응 단계
To a solution of 480 mg of potassium hydroxide in 40 ml of ethanol were added 2.0 g of α-methanesulfonyloxymethyl-β-(p-methoxyphenyl)-γ-butyrolactone and 1.6 ml of cyclohexylmercaptan and the resulting mixture was kept at room temperature for 4 hours. After completion of the reaction, the reaction mixture was diluted with 200 ml of ethyl ether, washed with water and saturated saline, dried over magnesium sulfate and the solvent was distilled off. The crude product thus obtained was purified by a silica gel column chromatography to give 600 mg (yield 22%) of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04613613 |
| 출처 데이터셋 | uspto-grants-1986_09 |
| ORD ID | ord-ba41b964acd849fab487151f8f23f48f |
| 출처 메모 | uspto-grants-1986_09 |