関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Chloride | HCID 5234 | — |
| 反応物 | tert-Butyl mercaptan | HCID 6387 | — |
| 反応物 | Bromopinacolone | HCID 21642 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 3,3-Dimethyl-1-tert.-butylthio-2-butanone | HCID 23349673 | — |
反応手順
To a solution of 5.8 g (0.25 m) of sodium metal in 175 ml of absolute ethanol is added, dropwise, 24.4 g (0.27 m) of 2-methyl-2propanethiol. The stirred solution is heated for 20 minutes, cooled, and treated in a dropwise manner with 44.8 g (0.25 m) of 1-bromopinacolone, prepared according to the procedure of J. Am. Chem. Soc., 74, 4507 (1952). This reaction mixture is heated at reflux for 20 minutes, cooled, and poured onto 200 g of ice and water. After being saturated with sodium chloride, the mixture is extracted with four portions of ether. The combined ether extracts are dried over anhydrous magnesium sulfate, filtered, and stripped of solvent. Distillation of the residue through a short Vigreaux column gives the desired product. Properties of this, and similar compounds prepared by substantially the same procedure using the appropriate mercaptans and α-haloketones, are given in Tables 1 and 2.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US03932471 |
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| 出典データセット | uspto-grants-1976_01 |
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| ORD ID | ord-28b138e8bb1a4cceaa1112c2343932af |
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| 出典メモ | uspto-grants-1976_01 |
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