HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 6-Chloro-4-(trifluoromethyl)pyridine-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | HCID 19066096 | HCID 19066096 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 6-Chloro-4-(trifluoromethyl)pyridine-2-carbonitrile | HCID 59570332 | — |
Reaction Steps
To 16 ml of acetonitrile were added 1.5 g of 2-chloro-4-trifluoromethylpyridine N-oxide, 2.12 ml of triethylamine, and 2.26 g of trimethylsilyl cyanide, and the mixture was heated to reflux for 23 hours. Thereafter, the reaction solution was allowed to cool to room temperature, and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.9 g of 2-chloro-6-cyano-4-trifluoromethylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318776B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-0aac6075075942b5b0b7dcab1f80c5cc |
| Source note | uspto-grants-2012_11 |