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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267596Generated: October 25, 2026

Hydrochloric Acid → 3-(2',4',5'-Triethoxybenzoyl)-trans-acrylic acid

https://huagongshe.com/reaction/267596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMaleic AnhydrideHCID 7923—
Reactant1,2,4-triethoxybenzeneHCID 179526—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon TetrachlorideHCID 5943—
Product3-(2',4',5'-Triethoxybenzoyl)-trans-acrylic acidHCID 12353591—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 2.1 parts by weight of 1,2,4-triethoxybenzene, 1.2 part by weight of maleic anhydride and 30 parts by volume of carbon tetrachloride is added 5.2 parts by weight of anhydrous aluminum chloride. The mixture is stirred for 1 hour and heated at 50°C for another 1 hour. After cooling, concentrated hydrochloric acid and ice are added to the mixture. The mixture is extracted with methylenechloride and the methylenechloride layer is washed with water and dried over anhydrous sodium sulfate. Upon removing the solvent by distillation, 3-(2',4',5'-triethoxybenzoyl)-trans-acrylic acid is obtained as crystals. Recrystallization from a mixture of ethanol and benzene gives yellow needles melting at 192°-194°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03943169
Source datasetuspto-grants-1976_03
ORD IDord-1cd74eb6cc8549da8a4f10f1779a543b
Source noteuspto-grants-1976_03