Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367768Generated: October 31, 2026

Benzyl Bromide → Benzene, [[(12-bromododecyl)oxy]methyl]-

https://huagongshe.com/reaction/1367768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant12-Bromo-1-dodecanolHCID 137895—
SolventTetrahydrofuranHCID 8028—
ProductBenzene, [[(12-bromododecyl)oxy]methyl]-HCID 1110033973%

Reaction Steps

12-Bromododecan-1-ol (1.83 g) was dissolved in 7 ml of dried THF, and sodium hydride (331.2 mg) was added to this solution. The reaction mixture was stirred at room temperature for 30 minutes, then benzyl bromide (0.99 ml) was added using a syringe, and the reaction mixture was refluxed for 24 hours while stirring. Saturated ammonium chloride solution was added to the reaction mixture, which was then extracted with diethyl ether. The organic layer was washed with saline solution, dried over magnesium sulfate, and filtered, and the solvent was distilled off under reduced pressure. Purification of the residue by silica gel flash chromatography (hexane:dichloromethane=8:2) gave 1-((12-bromododecanoxy)methyl)benzene as a colorless oil at a 73% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893304B2
Source datasetuspto-grants-2011_02
ORD IDord-d7bb9c06732b431d94ea8e06249d7b81
Source noteuspto-grants-2011_02