HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263113Generated: October 24, 2026
Sodium Chloride → 3,3-Dimethyl-1-tert.-butylthio-2-butanone
https://huagongshe.com/en/reaction/263113
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | tert-Butyl mercaptan | HCID 6387 | — |
| Reactant | Bromopinacolone | HCID 21642 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,3-Dimethyl-1-tert.-butylthio-2-butanone | HCID 23349673 | — |
Reaction Steps
To a solution of 5.8 g (0.25 mol) of sodium metal in 175 ml of absolute ethanol is added, dropwise, 24.4 g (0.27 mol) of 2-methyl-2-propanethiol. The stirred solution is heated for 20 minutes, cooled, and treated in a dropwise manner with 44.8 g (0.25 mol) 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 haloketones, are given in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04156082 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-7264d8d2c1274d419501d8848eafff6f |
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| Source note | uspto-grants-1979_05 |
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