HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (2E)-3-{4-[(ethoxycarbonyl)oxy]phenyl}prop-2-enoic acid
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 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2E)-3-{4-[(ethoxycarbonyl)oxy]phenyl}prop-2-enoic acid | HCID 12876666 | 98.4% |
Reaction Steps
67 g (0.41 mol) p-cumaric acid are added to a mixture of 50.4 g (0.90 mol) potassium hydroxide and 600 ml water. 53.1 g (0.50 mol) ethyl chloroformate are added dropwise at 0° C. The reaction temperature rises to 10° C. The reaction mixture is subsequently allowed to react for 2 hours at 25° C. and acidified to pH=1 with 200 ml hydrochloric acid 7N. The product is filtered off, washed with water and dried under vacuum to give 95.3 g of (2E)-3-{4-[(ethoxycarbonyl)oxy]phenyl}acrylic acid as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557922B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-552ab2648a5e453bb5132941afb9a79c |
| Source note | uspto-grants-2013_10 |