참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrogen Peroxide | HCID 784 | — |
| 반응물 | 2-Propanethiol | HCID 6364 | — |
| 반응물 | Chloroacetone | HCID 6571 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 촉매 | Sodium tungstate | HCID 26052 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-(Isopropylsulfonyl)propan-2-one | HCID 22908637 | 71.9% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05468589 |
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| 출처 데이터셋 | uspto-grants-1995_11 |
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| ORD ID | ord-cd3cc7551858402b927a8ff0ae3afcfc |
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| 출처 메모 | uspto-grants-1995_11 |
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