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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108206Generated: October 30, 2026

Benzyl Bromide → HCID 14642611, compound

https://huagongshe.com/reaction/2108206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant5-Hexen-1-olHCID 69963—
ProductHCID 14642611HCID 14642611—

Reaction Steps

To a stirred mixture of sodium hydride (2.6g, 110 mmoles) in tetrahydrofuran (185 ml) under a nitrogen atmosphere was added a solution of 5-hexene-1-ol (10g, 100 mmoles) in tetrahydrofuran (15 ml). After stirring at room temperature for 0.5 hour, the mixture was briefly heated to reflux and then cooled. Benzyl bromide (21.4 g, 125 mmoles) was added, and the mixture was stirred at reflux for one hour. Stirring was continued overnight at room temperature, after which the mixture was concentrated on a rotary evaporator. The mixture was poured into water, and the aqueous layer was extraced with three portions of ether. The combined organic estracts were dried over sodium sulfate, filtered, and the solvent evaporated. Chromatography of the residue on silica gel using a gradient of 0 to 10% ethyl acetate-hexane as eluant gave the title product (11.2 g) as an oil. The structure was confirmed by 1H NMR spectrometry.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04937357
Source datasetuspto-grants-1990_06
ORD IDord-fd43f93473b94b4ea87e8c3f1f751924
Source noteuspto-grants-1990_06