HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 2-Cyano-4-(trifluoromethyl)-5-pyrimidinecarbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Cyano-4-trifluoromethylpyrimidine-5-carboxylic acid | HCID 10584856 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Chlorine | HCID 24526 | — |
| Product | 2-Cyano-4-(trifluoromethyl)-5-pyrimidinecarbonyl chloride | HCID 10799769 | 83.1% |
Reaction Steps
A solution of 2-cyano-4-trifluoromethylpyrimidine-5-carboxylic acid (2.0 g, 9.2 mmol), oxalyl chloride (1.4 g, 11 mmol) and DMF (4 drops) in CH2 Cl2 (46 mL) was stirred at room temperature under N2 for 0.75 h. The reaction was concentrated and distilled (b.p. 100° C., 1.5 mm/Hg) to give the title compound (1.8 g, 82% yield); 1HNMR (CDCl3) δ 9.49 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811428 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-dd830d0144254084ac1e1e3106c68e28 |
| Source note | uspto-grants-1998_09 |