HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 1-Methyl 2-carboxybenzenepropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-(2-Carboxyphenyl)propionic acid | HCID 226294 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Methyl 2-carboxybenzenepropanoate | HCID 11790422 | — |
Reaction Steps
2-carboxybenzenepropanoic acid (9.7 g., 0.05 mole), acetic anhydride (15.5 g., 0.15 mole) and acetyl chloride (0.5 g) in dichloromethane (200 ml) was boiled at reflux under nitrogen for 16 hr. The solvents were removed at high vacuum and the residual cyclic anhydride was heated at reflux with methanol (250 ml) for 2 hrs. Evaporation of solvent gave the sub-title compound as an oil which crystallised with petroleum ether (b.p.60°-80°) to a solid (6.3 g) mp 76°-79°. This was further purified by continuous extraction of the crude product with boiling petroleum (b.p.40°-60°) in a Soxhlet apparatus. The pure compound, mp 79°-81° separated from the extracts on cooling.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04885313 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-297e8aa287434ff09466f2c5eced29e4 |
| Source note | uspto-grants-1989_12 |