HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523327Generated: October 25, 2026
Hydrochloric Acid → (2E)-3-{4-[(ethoxycarbonyl)oxy]phenyl}prop-2-enoic acid
https://huagongshe.com/reaction/523327
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | P-Coumaric Acid | HCID 637542 | — |
| Product | (2E)-3-{4-[(ethoxycarbonyl)oxy]phenyl}prop-2-enoic acid | HCID 12876666 | 83.6% |
Reaction Steps
67 g (400 mmol) of (2E)-3-(4-hydroxyphenyl)prop-2-enoic acid is added to a mixture of 57.4 g (880 mmol) of potassium hydroxide in 600 ml at 0° C. 46.6 mL (480 mmol) of ethyl chloridocarbonate are added dropwise so that the temperature is maintained to 10° C. The reaction mixture is subsequently allowed to react for 2 hours at 25° C. and then acidified to pH=1 with 200 mL of a 25% HCl solution- The precipitate is filtered off and washed with 500 mL of water. The residue is crystallized in 2 L of toluene and dried under vacuum to yield 79 g (74%) of pure (2E)-3-{4-[(ethoxycarbonyl)oxy]phenyl}prop-2-enoic acid as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334366B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-c19f24c05b9d478a89b10cc80c0ebf0b |
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| Source note | uspto-grants-2016_05 |
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