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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278418Generated: October 31, 2026

Propargyl bromide → 4-Cyclopropyl-4-hydroxy-1-octyne

https://huagongshe.com/reaction/1278418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactantn-Butyl cyclopropyl ketoneHCID 11029852—
SolventDiethyl EtherHCID 3283—
Product4-Cyclopropyl-4-hydroxy-1-octyneHCID 13078751—

Reaction Steps

To a stirred, refluxing suspension of amalgam prepared from 6.2 g of magnesium and 50 mg of mercuric chloride suspended in 60 ml of ether is added a solution of a mixture of 30.4 g n-butyl cyclopropyl ketone (Example 8) and 29.8 g of propargyl bromide in 65 ml of either during 60 minutes. After reaction at relfux temperature for an additional 30 minutes, the mixture is cooled to 0° and treated with 35 ml of saturated ammonium chloride. The mixture is diluted with ether and filtered through Celite. The filtrate is washed with brine, dried over potassium carbonate, and concentrated. The residue is distilled to provide a liquid, b.p. 93°-94° C. (12 mm), pmr spectrums (C D Cl3):δ0.43 (cyclopropyl hydrogens), 2.07 (triplet, HC≡C), and 2.44 (doublet, C=CCH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04281153
Source datasetuspto-grants-1981_07
ORD IDord-ccd478b16f594f048eddb8f491f006be
Source noteuspto-grants-1981_07