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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344244Generated: October 30, 2026

Benzyl Alcohol → ((4-Bromobutoxy)methyl)benzene

https://huagongshe.com/reaction/344244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantWaterHCID 962—
Reactant1,4-DibromobutaneHCID 8056—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product((4-Bromobutoxy)methyl)benzeneHCID 442218156.3%

Reaction Steps

60% Sodium hydride (1.2 g) was suspended in tetrahydrofuran (30 ml), and benzyl alcohol (3.0 g) was added under ice-cooling with stirring. The mixture was stirred at room temperature for 30 min, and again ice-cooled. 1,4-Dibromobutane (6.0 g) was added and the mixture was stirred for 3 hr. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried and the solvent was evaporated under reduced pressure to give 3.8 g of 4-benzyloxybutyl bromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05864039
Source datasetuspto-grants-1999_01
ORD IDord-89b52cc0d0794006be211b216e20e7b5
Source noteuspto-grants-1999_01