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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 848909생성일: 2026년 10월 24일

Propargyl bromide → 4-Hydroxy-4-methyl-7-oxa-1-octyne

https://huagongshe.com/ko/reaction/848909

반응식

참여 물질

역할이름HCID투입량
반응물Propargyl bromideHCID 7842—
반응물2-Butanone, 4-methoxy-HCID 138889—
반응물MagnesiumHCID 5462224—
반응물HCID 178455849HCID 178455849—
용매Diethyl EtherHCID 3283—
생성물4-Hydroxy-4-methyl-7-oxa-1-octyneHCID 12786229—

반응 단계

To a stirred solution of propargylmagnesium bromide in 35 ml. of ether, prepared from 7.65 g. (0.3 moles) of magnesium, 170 mg. of mercuric chloride and 33.6 g. (0.28 moles) of propargyl bromide, is added dropwise under argon atmosphere a solution of 25 g. (0.245 moles) of 4-methoxy-2-butanone [L. R. Fedor, J. Am. Chem. Soc., 91:4, 908 (1969)] in 20 ml. of ether at a rate to maintain gentle refluxing. The resulting mixture is stirred at ambient temperature for an additional 30 minutes then quenched at 5° C. by the addition of 140 ml. of saturated ammonium chloride solution. After filtration the ether phase is separated; the aqueous phase is extracted twice with additional ether. The combined ether extracts are washed with saturated sodium chloride solution, dried with anhydrous magnesium sulfate and taken to dryness in vacuo. Distillation of the residual oil provided 13.7 g. (40%) of product; b.p. 84°-85° C. (13 mm.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04297516
출처 데이터셋uspto-grants-1981_10
ORD IDord-94de3cf87cb64ef48b91e77c406ba337
출처 메모uspto-grants-1981_10