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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255774Generated: October 30, 2026

Benzyl Bromide → 35085-32-6

https://huagongshe.com/reaction/2255774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
SolventDimethylformamideHCID 6228—
Product35085-32-6HCID 27008940.7%

Reaction Steps

2.1 g of sodium hydride (60% in oil) was suspended in DMF, and 10 g of ethyl diethylphosphonoacetate was dropwise added thereto at -20° C. under argon atmosphere. The mixture was stirred at room temperature for 30 minutes, and then 9.2 g of benzyl bromide was added thereto at 0° C. The mixture was stirred at 50° C. overnight. The reaction solution was poured into a saturated ammonium chloride aqueous solution, and extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated sodium chloride aqueous solution, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/acetone=6/1) to obtain 5.7 g of ethyl 2-diethylphosphono-3-phenylpropionate as colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240924
Source datasetuspto-grants-1993_08
ORD IDord-3ee25a42c00048ce8c198540f06103e6
Source noteuspto-grants-1993_08