HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → p-Ethoxycarbonylbenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Terephthaloyl chloride | HCID 7488 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | p-Ethoxycarbonylbenzoyl chloride | HCID 12276626 | — |
Reaction Steps
p-Ethoxycarbonylbenzoyl chloride is prepared according to the method of M. J. Dewar and J. P. Schroeder, J. Org. Chem., 30, 2297 (1965), by the gradual addition of a small amount of ethyl alcohol to a boiling solution of terephthaloyl chloride in benzene. After removal of the solvent the residue is distilled under reduced pressure to give the acyl chloride which boils at 102°-105° C. at 0.4 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04011236 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-a7b530671e9640e78a772d5fe112c8ba |
| Source note | uspto-grants-1977_03 |