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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963573Generated: October 25, 2026

Allyl bromide → 2-[4-Fluorophenyl]ethyl allyl ether

https://huagongshe.com/reaction/963573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant4-Fluorophenethyl AlcoholHCID 82068—
SolventDimethylformamideHCID 6228—
Product2-[4-Fluorophenyl]ethyl allyl etherHCID 1908228497.3%

Reaction Steps

2-[4-Fluorophenyl]ethanol (7.0 g) was added slowly to a stirred suspension of sodium hydride (1.25 g, 60% as dispersion in oil prewashed with petroleum ether bp 60°-80°) in DMF (50 ml). The mixture was stirred for 30 min at room temperature. Allyl bromide (6.0 g) was then added slowly and the whole allowed to stir overnight. The reaction was partitioned between water and ether. The aqueous layer was further extracted with ether and the combined ethereal extracts were washed with water and dried (MgSO4). The ether was removed under reduced pressure to yield the crude subtitled compound as a colourless oil (8.7 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763465
Source datasetuspto-grants-1998_06
ORD IDord-38ddd61b2c5c4824a08344edaecd409e
Source noteuspto-grants-1998_06