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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065168Generated: October 25, 2026

Propargyl bromide → 7-Chloro-4-hydroxy-4-methyl-1-heptyne

https://huagongshe.com/reaction/1065168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
Reactant1,1-DibromoethaneHCID 11201—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Pentanone, 5-chloro-HCID 79993—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product7-Chloro-4-hydroxy-4-methyl-1-heptyneHCID 12898739—

Reaction Conditions

Temperature-5 °C

Reaction Steps

To a mixture of 6.69 g. of magnesium in 20 ml. of ether under argon, is added 0.1 g. of mercuric chloride and 0.1 g. of dibromoethane. The mixture is stirred for 10 minutes and 0.5 ml. of propargyl bromide is added. A 50 ml. portion of ether is added, followed by a solution of 30 g. of 5-chloro-2-pentanone and 32.55 g. of propargyl bromide in 45 ml. of ether with stirring, at a rate to maintain vigorous reflux. The mixture is stirred an additional 15 minutes, cooled to -5° C. and an ice cold saturated solution of ammonium chloride is added dropwise. The ether layer is decanted and filtered. The solids are washed with ether which is also filtered. The combined ether filtrates are washed with water, dried over magnesium sulfate and the solvent removed giving the product as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04328359
Source datasetuspto-grants-1982_05
ORD IDord-eba18b520af340e3b409c3c092e29947
Source noteuspto-grants-1982_05