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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714588Generated: October 25, 2026

Sodium Carbonate → Ethyl 3-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]acrylate

https://huagongshe.com/reaction/1714588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium BicarbonateHCID 516893—
Reactant4-(3-Benzyloxyphenylthio)-2-chlorobenzaldehydeHCID 16655405—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]acrylateHCID 59464778—

Reaction Steps

A mixture of 4-(3-benzyloxyphenylthio)-2-chlorobenzaldehyde (1) and ethyl diethylphosphonoacetate (2) is stirred for 3 to 8 hours at 50 to 80° C. in an organic solvent, such as dimethylformamide or dimethylsulfoxide, in the presence of a base, such as potassium bicarbonate, sodium bicarbonate, potassium carbonate or sodium carbonate. Subsequently, the reaction mixture is chilled in an ice water bath while being stirred and water is added. The resulting crystals are collected by filtration and washed with aqueous 2-propanol to give ethyl 3-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]acrylate (3) as crude crystals. This product is dissolved in ethylacetate and the mixture was washed with water. The organic layer is concentrated under reduced pressure to obtain a pale yellow oil. To this product, acetone is added and the mixture is stirred while being chilled to form crystals (Crystal seeds are added when necessary). Water is then added and the mixture is stirred while being chilled. The resulting crystals are collected by filtration and washed with acetone-water. The crystals are then dried at 40° C. or below to give ethyl 3-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]acrylate (3) or a hydrate thereof.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795472B2
Source datasetuspto-grants-2010_09
ORD IDord-4a062d7335ec45b58e606242b48284ca
Source noteuspto-grants-2010_09