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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663560Generated: October 30, 2026

3-Chlorobenzaldehyde → Ethyl 3-(3-chlorophenyl)-2-propenoate

https://huagongshe.com/reaction/1663560

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorobenzaldehydeHCID 11477—
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(3-chlorophenyl)-2-propenoateHCID 36720392%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 2 l three necked flask fitted with mechanical stirrer and dropping funnel under inert atmosphere, 106.2 g (755 mmoles, 1 eq) of 3-chlorobenzaldehyde are dissolved in 1 l of THF and cooled down to 0° C. 341.9 g (980 mmoles, 1.3 eq) of ethyl (triphenylphosphoranylidene)acetate are then added under efficient stirring, the temperature raising to 10° C. The mixture is kept under stirring one hour at 0° C., and then overnight at room temperature. The mixture is concentrated to dryness, the residue suspended in diethyl ether, the triphenylphosphine oxide is filtered off and the filtrate concentrated to dryness. The residue is purified by PrepLC (1 kg SiO2, pet. ether/EtOAc, 75:35) to give 191.8 g of pure 375, 92% yield. 1H NMR (250 MHz, (CD3)2SO): 1.30 (t, 3H), 4.25 (q, 2H), 6.70 (d, 1H), 7.40 (m, 2H), 7.50-7.70 (m, 2H), 7.85 (s(broad), 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034958B2
Source datasetuspto-grants-2011_10
ORD IDord-30432ab6953e43109a85315a6390d63b
Source noteuspto-grants-2011_10