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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36456Generated: October 30, 2026

Benzyl Bromide → Tert.butyl(benzyl)(diethoxymethyl)phosphine oxide

https://huagongshe.com/reaction/36456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178472281HCID 178472281—
SolventTetrahydrofuranHCID 8028—
ProductTert.butyl(benzyl)(diethoxymethyl)phosphine oxideHCID 19938721—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Tertiary-butyl(diethoxymethyl)phosphine oxide (2.5 g), (0.012 mol) is dissolved in 35 ml of dry tetrahydrofuran and cooled to -78° C. under an argon atmosphere. To this stirred solution is added 9.0 ml of n-butyl lithium (1.6M solution in hexane) and the mixture is stirred at -78° C. for 10 minutes. After this time, a solution of 2.47 g (0.014 mol) of benzyl bromide in 15 ml of dry tetrahydrofuran is added, and the reaction mixture is allowed to warm to room temperature. After stirring for 3 hours at room temperature, 10 ml of saturated ammonium chloride solution is added and the product is extracted into diethyl ether (2×100 ml). The combined organic extracts are dried and evaporated under reduced pressure to give a crude product. This is purified by chromatography on silica, using ethyl acetate as eluent, to give tertiary-butyl(benzyl)(diethoxymethyl) phosphine oxide as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05414133
Source datasetuspto-grants-1995_05
ORD IDord-baa62213048349e786b517c85532daf9
Source noteuspto-grants-1995_05