Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Cyclopentanol → Cyclopentyl 4-methylbenzene-1-sulfonate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Cyclopentanol | HCID 7298 | — |
| 반응물 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | Cyclopentyl 4-methylbenzene-1-sulfonate | HCID 317685 | 81.8% |
반응 단계
Cyclopentanol (10 g, 0.116 mol), p-toluenesulfonyl chloride (24.8 g, 0.128 mol) and ether (100 ml) were charged into a 200 cc round-bottom flask and dissolved. Then, potassium hydroxide (32.5 g, 0.58 mol) in a powder form was added slowly thereto while cooling below 10° C. in a water bath. After addition, the mixture was stirred as it was for additional 2 hours. After completion of the reaction, the mixture was poured into ice-water (20 ml), and the organic layer and the aqueous layer were separated. The organic layer was dried, and concentrated under reduced pressure to obtain cyclopentyl p-toluenesulfonate as a pale yellow viscous liquid (22.0 g, 81.8% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05424277 |
| 출처 데이터셋 | uspto-grants-1995_06 |
| ORD ID | ord-59bf7bd3f4e34541b45f75089796faf8 |
| 출처 메모 | uspto-grants-1995_06 |