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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | 1,2,4-triethoxybenzene | HCID 179526 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-(2',4',5'-Triethoxybenzoyl)-trans-acrylic acid | HCID 12353591 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03943169 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-1cd74eb6cc8549da8a4f10f1779a543b |
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| Source note | uspto-grants-1976_03 |
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