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Acetic Acid → alpha-Mercaptomethyl-beta-phenyl-gamma-butyrolactone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Sodium hydrosulfide | HCID 28015 | — |
| 反応物 | beta-(p-Chlorophenyl)-alpha-methanesulfonyloxymethyl-gamma-butyrolactone | HCID 13518915 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | alpha-Mercaptomethyl-beta-phenyl-gamma-butyrolactone | HCID 13518975 | 52% |
反応手順
To a solution of 1.0 g of α-methanesulfonyloxymethyl-β-phenyl-γ-butyrolactone (III) in 20 ml of ethanol were added 1.5 ml of acetic acid and then 1.2 g of commercially available 70% sodium hydrosulfide and the mixture was stirred at room temperature for 18 hours. After completion of the reaction, the reaction mixture was diluted with 150 ml of ethyl acetate, washed with water in a conventional manner, dried over magnesium sulfate and the solvent was distilled off. The crude product thus obtained was purified by a column chromatography to give 400 mg (yield 52%) 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-62844afc2adb4bd9bea5546d1bc4665b |
| 出典メモ | uspto-grants-1986_09 |