HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → Methyl 3-(trifluoromethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | 3-(Trifluoromethyl)benzoic acid | HCID 9963 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 3-(trifluoromethyl)benzoate | HCID 520213 | 97.8% |
Reaction Steps
An excess solution of diazomethane in ether was added to an ice-cooled and stirred solution of m-trifluoromethylbenzoic acid (8.0 g, 42.1 mmol) in 50 ml of ether. After concentration, the residue was distilled under reduced pressure to give a colorless transparent oil of methyl m-trifluoromethylbenzoate (8.4 g, 41.2 mmol, yield 97.8%, b.p. 76°-78° C./12 mmHg), which was assigned the structure by the following data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04775692 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-d64fff4c7fa64ce4ab94f1133f1298f5 |
| Source note | uspto-grants-1988_10 |