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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453243Generated: October 29, 2026

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

https://huagongshe.com/reaction/453243

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 triphenylphospine 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 numberUS08492416B2
Source datasetuspto-grants-2013_07
ORD IDord-e26c1222770e4e76b62cb08c6f4bda0c
Source noteuspto-grants-2013_07