HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → Acetic acid 4-chlorocarbonyl-2,6-dimethyl-phenyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3,5-Dimethyl-4-acetoxybenzoic acid | HCID 18704189 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Acetic acid 4-chlorocarbonyl-2,6-dimethyl-phenyl ester | HCID 18704177 | — |
Reaction Steps
To a solution of 4-acetoxy-3,5-dimethylbenzoic acid (2.08 g, 10.0 mmol) in anhydrous dichloromethane (40 mL) were sequentially added oxalyl chloride (3.81 g, 30.0 mmol) and anhydrous DMF (5 drops). The reaction mixture was stirred at room temperature for 6 hours. Solvent and excess oxalyl chloride were evaporated under reduced pressure and the residue was dried under vacuum to give acetic acid 4-chlorocarbonyl-2,6-dimethylphenyl ester (3) as an orange solid. Yield: 2.32 g (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952021B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-e5691963917d42f188b6de7a88cd610f |
| Source note | uspto-grants-2015_02 |