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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2169생성일: 2026년 10월 23일

Formaldehyde → 3-Cyclohexylprop-2-yn-1-ol

https://huagongshe.com/ko/reaction/2169

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물EthynylcyclohexaneHCID 70263—
용매Diethyl EtherHCID 3283—
생성물3-Cyclohexylprop-2-yn-1-olHCID 316601—

반응 단계

To a solution of ethyl magesium bromide (prepared from 2.5 g of magnesium turning and 11.3 g of bromoethane) in ether was added dropwise a solution of 10.2 g of cyclohexylacetylene in ether and the reaction mixture was refluxed for 2 hours. The reaction mixture was cooled to ambient temperature and anhydrous formaldehyde (prepared from the thermal decomposition of 50 g of paraformaldehyde for 20 minutes) was bubbled into the mixture. After cooling, the reaction was quenched with saturated ammonium chloride and extracted with ether (2×100 ml). The combined ether extracts were washed with brine, dried over magnesium sulfate and evaporated to yield the product which was distilled under high vacuum at 68°-74° C. to yield 6.4 g as a colorless liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728715
출처 데이터셋uspto-grants-1998_03
ORD IDord-b7fb0104fad94bc0b378012d50f6c0c8
출처 메모uspto-grants-1998_03