HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → (3-(Chlorocarbonyl)-2-methylphenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Acetoxy-2-methylbenzoic acid | HCID 3798557 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | (3-(Chlorocarbonyl)-2-methylphenyl)acetate | HCID 7010345 | 100% |
Reaction Steps
3-Acetoxy-2-methylbenzoic acid was slurried in methyl-t-butyl ether (MTBE) and treated with 1.2 equivalents of thionyl chloride and catalytic dimethylformamide. After three hours at ambient temperatures, the reaction was complete, giving a brown solution. Solvent (MTBE) was removed by vacuum distillation. Residual thionyl chloride was removed by addition of toluene followed by vacuum distillation. The resulting 3-acetoxy-2-methylbenzoyl chloride was isolated either directly as an oil or by crystallization from two volumes of heptane at <10° C. Product was obtained in >100% yield when isolated as an oil and 82-85% yield when crystallized from heptane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06303786B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-4ea5497c65bb4ac8974784950293d6cf |
| Source note | uspto-grants-2001_10 |