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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21481생성일: 2026년 10월 26일

Cyclopentanol → Cyclopentyl 4-methylbenzene-1-sulfonate

https://huagongshe.com/reaction/21481

반응식

참여 물질

역할이름HCID투입량
반응물CyclopentanolHCID 7298—
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물Potassium HydroxideHCID 14797—
용매Diethyl EtherHCID 3283—
생성물Cyclopentyl 4-methylbenzene-1-sulfonateHCID 31768581.8%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424277
출처 데이터셋uspto-grants-1995_06
ORD IDord-59bf7bd3f4e34541b45f75089796faf8
출처 메모uspto-grants-1995_06