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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848909Generated: October 25, 2026

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

https://huagongshe.com/reaction/848909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
Reactant2-Butanone, 4-methoxy-HCID 138889—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178455849HCID 178455849—
SolventDiethyl EtherHCID 3283—
Product4-Hydroxy-4-methyl-7-oxa-1-octyneHCID 12786229—

Reaction Steps

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.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04297516
Source datasetuspto-grants-1981_10
ORD IDord-94de3cf87cb64ef48b91e77c406ba337
Source noteuspto-grants-1981_10