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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649788Generated: November 3, 2026

Propargyl alcohol → 1-Bromo-6-(prop-2-YN-1-yloxy)hexane

https://huagongshe.com/reaction/1649788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
Reactant1,6-DibromohexaneHCID 12368—
ReactantSodium HydroxideHCID 14798—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
Product1-Bromo-6-(prop-2-YN-1-yloxy)hexaneHCID 2189550168.5%

Reaction Steps

A mixture of propargyl alcohol (5.6 g), 1,6-dibromohexane (73.2 g), tetrabutylammonium bisulphate (0.5 g), and aqueous sodium hydroxide (50%, w/v, 27 ml) was stirred at room temperature for 20 h, diluted with water (50 ml), and extracted with diethyl ether (2×100 ml). The dried extract was evaporated and the residue was purified on a column of silica (Merck 9385) eluting with cyclohexane followed by cyclohexane-diethyl ether (19:1) to give the title compound as a colourless oil (15.0 g), t.l.c. (cyclohexane-diethyl ether 9:1) Rf 0.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921867
Source datasetuspto-grants-1990_05
ORD IDord-4c22af32127b4a9c902ac0aba2d21e79
Source noteuspto-grants-1990_05