HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328922Generated: October 26, 2026
Hydrochloric Acid → 4-(2-Carboxyethyl)benzalacetophenone
https://huagongshe.com/reaction/328922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | 3-(4-Formylphenyl)propanoic acid | HCID 19825241 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-(2-Carboxyethyl)benzalacetophenone | HCID 54386652 | 100% |
Reaction Steps
To a solution of 5.34 g of 4-formyldihydrocinnamic acid in 50 ml of 1N sodium hydroxide was added a solution of 3.6 g of acetophenone and 20 ml of ethanol. The reaction mixture was stirred at room temperature for 4 hrs. and then poured onto 300 g of crushed ice. 1N Hydrochloric acid was added and, after stirring at 0° C for 15 min., the precipitate was collected and washed with water. The precipitate was dissolved in 500 ml of ethyl acetate, dried over anhydrous sodium sulfate and the drying agent was collected on a filter. The filtrate was concentrated to about 100 ml and seeded with crystalline product. The solid was collected, washed with 1:4-ethyl acetate-ether followed by ether and dried at 70°-75° C under vacuum to give 8.4 g (72%) of 4-(2-carboxyethyl)benzalacetophenone, as yellow needles, m.p. 159°-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04018884 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-8ffc4ecec4f142dbbf54f60e10477700 |
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| Source note | uspto-grants-1977_04 |
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