HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic anhydride → 2-Bromo-4-fluorobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 2-Bromo-4-fluorobenzamide | HCID 20372234 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Bromo-4-fluorobenzonitrile | HCID 118939 | — |
Reaction Steps
A solution of 10.9 g. (0.05 mole) of 2-bromo-4-fluorobenzamide in 50 ml. of dry pyridine is stirred and cooled in an ice-bath while 11.2 g. (0.0525 mole) of trifluoroacetic anhydride is added dropwise. After 2 hours at room temperature, the bulk of the solvent is evaporated under reduced pressure and the residue is dissolved in ether. Evaporation of the washed and dried ethereal extract under reduced pressure leaves the product as the residual solid. Sublimation at 55°C. and 0.05 mm. yields white crystals, m.p. 75°-76.5°C. A sample from a previous experiment was resublimed for analysis, m.p. 77°-78°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03978127 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-4a7855118ec5449eab8f20a11467c798 |
| Source note | uspto-grants-1976_08 |