HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129375Generated: October 25, 2026
Hydrogen Peroxide → 1-(Isopropylsulfonyl)propan-2-one
https://huagongshe.com/reaction/129375
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 2-Propanethiol | HCID 6364 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | Sodium tungstate | HCID 26052 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(Isopropylsulfonyl)propan-2-one | HCID 22908637 | 71.9% |
Reaction Steps
To 2-propanethiol (12.2 g, 0.16 mole), a solution of potassium hydroxide (11.5 g, 0.174 mole) in ethanol (100 ml) was added dropwise at 15° C. or lower, and continued to stir at the same temperature for 24 hours. Then chloroacetone (23.1 g, 0.25 mole) was added dropwise at 10°-15° C., and reacted with stirring at 20° C. for 4 hours. To this mixture, sodium tungstate (0.8 g) was added, 30% hydrogen peroxide (36 g, 0.32 mole) was added dropwise at 45°-55° C., and reacted with stirring at room temperature for 14 hours. The reaction mixture was extracted with methylene chloride (200 ml). The organic layer was washed with H2O, dried over anhydrous MgSO4 and evaporated to give 18.9 g of residual crude 1-(1-methylethylsulfonyl)acetone as a brownish yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05468589 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-cd3cc7551858402b927a8ff0ae3afcfc |
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| Source note | uspto-grants-1995_11 |
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