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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837629Generated: October 31, 2026

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

https://huagongshe.com/reaction/1837629

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 1I 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), (s(broad), 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784197B2
Source datasetuspto-grants-2004_08
ORD IDord-1d9680e64d144d6fab460406dbbac56c
Source noteuspto-grants-2004_08