참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Chlorosulfonic acid | HCID 24638 | — |
| 반응물 | Tricyclohexylbenzene | HCID 3015433 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Sodium 1,3,5-tricyclohexylbenzenesulfonate | HCID 86655172 | 151.4% |
반응 단계
In 50 ml of methylene chloride, 30 g of tricyclohexylbenzene was dissolved, cooled by 3° C. and stirred, and 15.2 g of chlorosulfonic acid was slowly added dropwise. After the dropwise addition, the mixture was stirred for 5 hours at room temperature, and after the introduction of 10 g of ice, 40 g of 50% aqueous sodium hydroxide was introduced. After a further 20 g of ethanol was added and stirring for 1 hour at 50° C., the undissolved portion was filtered off and removed and the mixture was distilled off at reduced pressure at 40° C. The precipitated crystals were filtered off and washed with hexane, and 30 g of sodium 1,3,5-tricyclohexylbenzensulfonate was obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08673538B2 |
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| 출처 데이터셋 | uspto-grants-2014_03 |
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| ORD ID | ord-9e5d705099234d509ed3486e771fbf63 |
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| 출처 메모 | uspto-grants-2014_03 |
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