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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107265Generated: October 25, 2026

Tetrahydrofuran → Ethyl 3-(2-anilinothiazol-4-yl)acrylate

https://huagongshe.com/reaction/2107265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
Reactant2-Anilinothiazole-4-carbaldehydeHCID 15053570—
SolventWaterHCID 962—
ProductEthyl 3-(2-anilinothiazol-4-yl)acrylateHCID 54052926—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture comprising 3.5 g of 2-anilinothiazole-4-carbaldehyde, 6.5 g of (ethoxycarbonylmethylene)triphenylphosphorane and 35 ml of tetrahydrofuran was heated at 60 ° C. for 2 hours. The reaction mixture was poured into water and extracted with benzene. The benzene extract was dried over anhydrous sodium sulfate, and the solvent was evaporated off under reduced pressure, giving an oil. This oil was purified by silica gel column chromatography. using as eluent a 9:1 mixture of benzene and ethyl acetate, giving the desired compound as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933355
Source datasetuspto-grants-1990_06
ORD IDord-7f3200267c1946fc93d2bec920aa06e4
Source noteuspto-grants-1990_06