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HRID 46738생성일: 2026년 10월 24일

Cycloheptene → 2-[(1-Cyclohepten-3-yl)thio]acetaldehyde

https://huagongshe.com/ko/reaction/46738

반응식

참여 물질

역할이름HCID투입량
반응물CyclohepteneHCID 12363—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
용매Propan-2-one--water (1/1)HCID 18366337—
생성물2-[(1-Cyclohepten-3-yl)thio]acetaldehydeHCID 12620961100%

반응 단계

A solution of 108.13 g (0.443 mole) of 3-[2,2-diethoxyethyl)thio]-1-cycloheptene in 1000 ml of acetone/water, 9:1 was treated with 1.1 g of p-toluenesulfonic acid hydrate and heated under reflux for 1.0 hour, cooled, and concentrated. The residue was partitioned between ether/10% sodium bicarbonate. The aqueous phase was further extracted with ether. The organic extracts were pooled, dried over magnesium sulfate, and evaporated to afford 75.30 g (0.443 mole, 100%) of 2-[(1-cyclohepten-3-yl)thio]acetaldehyde as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04175086
출처 데이터셋uspto-grants-1979_11
ORD IDord-d2e4355203d449d08f1cb4c0210246dc
출처 메모uspto-grants-1979_11