Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118191Generated: October 25, 2026

Diethyl Ether → 1-Bromo-7-(prop-2-yn-1-yloxy)heptane

https://huagongshe.com/reaction/2118191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPropargyl alcoholHCID 7859—
ReactantSodium HydroxideHCID 14798—
Reactant1,7-DibromoheptaneHCID 78309—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
Product1-Bromo-7-(prop-2-yn-1-yloxy)heptaneHCID 2189554017%

Reaction Conditions

Temperature60 °C

Reaction Steps

25% (w/w) aq. NaOH (700 ml) was added to a stirred mixture of propargyl alcohol (70 g), tetra-butyl ammonium bromide (3.5 g) and 1,7-dibromoheptane (322 g) maintaining the temperature below 30° C. The reaction mixture was heated at 60° C. for 5 hrs then allowed to cool to room temperature and stirred overnight. Diethyl ether (350 ml) and water (280 ml) were added, the mixture stirred and allowed to settle. The aqueous layer was extracted with diethyl ether (210 ml), the organic layers combined, dried (MgSO4). The solution was concentrated to give 280 g of crude material. 140 g Of the crude was purified by chromatography on Biotage (800 g) eluting with petroleum ether then petroleum ether:ethyl acetate (100:1 followed by 100:1.5) to give the title compound (49.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442836B2
Source datasetuspto-grants-2008_10
ORD IDord-e0913e33394e4054831f8898cba53acb
Source noteuspto-grants-2008_10