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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283262Generated: October 27, 2026

Diethyl chlorophosphate → 1-Bromo-4-[(E)-2-ethoxysulfonylethenyl]benzene

https://huagongshe.com/reaction/2283262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl chlorophosphateHCID 13139—
Reactant4-BromobenzaldehydeHCID 70741—
Reactant1-PropanesulfonateHCID 4431756—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-4-[(E)-2-ethoxysulfonylethenyl]benzeneHCID 8663200264%

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyllithium (59.0 mL, 1.6M solution in hexanes) was added dropwise during 25 min to a solution of ethylmethanesulfonate (9.1 mL, 86 mmol) in THF (200 mL) at −78° C. The reaction mixture was stirred for 15 min then diethyl chlorophosphate (7.2 ml, 50 mmol) was added dropwise. The solution was stirred at −78° C. for 30 min, allowed to warm to 0° C. and then cooled to −78° C. again. 4-Bromobenzaldehyde (9.2 g, 50 mmol) in THF (50 mL) was then added dropwise during 15 minutes and the resulting mixture was then allowed to slowly reach RT and stirred overnight. Water (20 mL) was added to the mixture and the reaction was concentrated in vacuo. The residue was extracted with diethyl ether and the combined organic extracts were washed with aqueous saturated sodium chloride, dried over magnesium sulfate, filtered and the solvent was evaporated in vacuo. Purification by column chromatography, using 15% ethyl acetate/hexanes as the eluent, afforded the title compound (9.3 g, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-e6e13d12bb50468b8e062189a5b6d9dd
Source noteuspto-grants-2015_09