HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → Methyl 2-chloro-5-(trifluoromethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Chloro-5-(trifluoromethyl)benzoic acid | HCID 688182 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-chloro-5-(trifluoromethyl)benzoate | HCID 15010065 | 100.4% |
Reaction Steps
To a solution of 2-chloro-5-(trifluoromethyl)benzoic acid (15 g, 66.8 mmol) in methylene chloride (200 mL) was added oxalyl chloride (12.7 g, 100 mmol) drop wise followed by the addition of 5-6 drops of DMF. The reaction mixture was concentrated, the residue partitioned between methylene chloride and 5% aq. sodium carbonate. The organic layer was dried (MgSO4) and concentrated to give the title compound as a pale oil (16 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07572805B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-bea4f7d9b8614ef2b3354384d0dc7cad |
| Source note | uspto-grants-2009_08 |