HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetic Acid → HCID 343978, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetic Acid | HCID 999 | — |
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 343978 | HCID 343978 | — |
Reaction Steps
A mixture of 56.2 g 4-chlorobenzaldehyde, 54.4 g phenylacetic acid, 80 ml acetic anhydride and 40 ml triethylamine was refluxed for 5 hours. Unreacted 4-chlorobenzaldehyde was removed by steam distillation and the residue dissolved in aqueous alcohol and treated with decolourising carbon. Crystals of α-phenyl-4-chlorocinnamic acid were obtained on acidification of the solution. The product was recrystallised from alcohol and found to have a melting point of 202°-4° C. The chlorosulphonyl derivative was prepared according to the method described in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04254244 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-3c9d1d525c4241308f4373461fe5957a |
| Source note | uspto-grants-1981_03 |