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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957101Generated: November 1, 2026

Phenethyl bromide → HCID 19068911, compound

https://huagongshe.com/reaction/1957101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
Reactanttert-Butyl DimethylphosphonoacetateHCID 4564495—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductHCID 19068911HCID 1906891160.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

118 g of tert-butyl dimethylphosphonoacetate were dissolved, under a nitrogen atmosphere, in 875 ml of dry dimethylformamide. 58.9 g of potassium tert-butoxide were added to the solution while cooling with ice. The reaction mixture was subsequently heated at 60° C. for a short period and then allowed to cool down to room temperature. A solution of 104.9 g of phenethyl bromide in 110 ml of dimethylformamide was added dropwise to the reaction mixture. The reaction mixture was then heated at 60° C. for 2 hours. For the working-up, most of the dimethylformamide was evaporated under reduced pressure and the remaining residue was dissolved in methyl tert-butyl ether. The solution was acidified with aqueous potassium hydrogen sulfate solution. The organic phase was then separated, washed with water, dried over sodium sulfate and evaporated under reduced pressure. The resulting crude product was purified by flash chromatography on 3 kg of silica gel using dichloromethane/methyl tert-butyl ether (4:1) as the eluent. 105.1 g of pure tert-butyl 2-(dimethylphosphono)-4-phenyl-n-butyrate were obtained as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783573
Source datasetuspto-grants-1998_07
ORD IDord-e54536ea9c5442a69197058d320a0bbf
Source noteuspto-grants-1998_07