HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623315Generated: October 31, 2026
Ethyl Acetate → 4-Chloro-6-(trifluoromethyl)-3-pyridineacetonitrile
https://huagongshe.com/reaction/623315
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 72212581 | HCID 72212581 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Chloro-6-(trifluoromethyl)-3-pyridineacetonitrile | HCID 86732544 | 65.1% |
Reaction Steps
Trimethylsilylcyanid (TMSCN) (69.3 g, 0.7 mol) was added to a solution of 4-chloro-5-(chloromethyl)-2-(trifluoromethyl)pyridine (Int-13) (80 g, 0.348 mol) and Tetra-n-butylammoniumfluoride (129.5 g, 0.7 mol) in acetonitrile (1.5 L) slowly. Then the mixture was stirred at 20-30° C. for 2 hours. Thin layer chromatography (petroleum ether: EtOAc=3:1) showed all of starting material was consumed. The mixture was concentrated and the residue was purified by silica gel chromatography eluted with petroleum ether: EtOAc=20:1˜3:1 to yield [4-chloro-6-(trifluoromethyl)pyridin-3-yl]acetonitrile (Int-14) (50 g, 60% from NMR, 39% of yield) as yellow syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09301526B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-f2f344c87c9d4a30a72092f6ede91c52 |
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| Source note | uspto-grants-2016_04 |
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