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Potassium Hydroxide → alpha-Cyclohexylthiomethyl-beta-(p-methoxyphenyl)-gamma-butyrolactone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | Cyclohexanethiol | HCID 15290 | — |
| 反応物 | alpha-Methanesulfonyloxymethyl-beta-(p-methoxyphenyl)-gamma-butyrolactone | HCID 20234197 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | alpha-Cyclohexylthiomethyl-beta-(p-methoxyphenyl)-gamma-butyrolactone | HCID 13518978 | 22% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04613613 |
| 出典データセット | uspto-grants-1986_09 |
| ORD ID | ord-ba41b964acd849fab487151f8f23f48f |
| 出典メモ | uspto-grants-1986_09 |