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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283264Generated: October 30, 2026

4-Chlorobenzaldehyde → HCID 86632003, compound

https://huagongshe.com/reaction/2283264

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantDiethyl chlorophosphateHCID 13139—
ReactantEthanesulfonic acid, ethyl esterHCID 74704—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86632003HCID 8663200358%

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyllithium (35.0 mL, 1.6M solution in hexanes) was added dropwise during 25 min to a solution of ethyl ethanesulfonate (6.9 g, 50 mmol) (Synth. Comm. 1985, 15, 1057) in THF (100 mL) at −78° C. The reaction mixture was stirred for 15 min then diethyl chlorophosphate (4.35 ml, 30 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-Chlorobenzaldehyde (4.2 g, 30 mmol) in THF (30 mL) was then added dropwise during 15 minutes and the resulting mixture was stirred for 1 h at −78° C. and then allowed to slowly reach RT. Water (10 mL) was added to the mixture and the mixture 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 a gradient of 10% ethyl acetate/hexanes to 15% ethyl acetate/hexanes as eluent, afforded the title compound (4.5 g, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-42ec0d07c4f04328af99108c7aa7b162
Source noteuspto-grants-2015_09