Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoroiodomethane | HCID 16843 | — |
| Product | Trifluoromethylpyridine | HCID 136199 | 19.9% |
Reaction Steps
In the same reaction vessel as used in Example 1, 15.82 g of pyridine and 7.83 g of trifluoromethyl iodide were mixed. The vessel was airtightly sealed and heated at 180° C. for 24 hours. After the reaction, the reactor was cooled to room temperature. Thereafter, the reaction mixture was removed from the cooled vessel and treated by following the procedure of Example 1. Consequently, there was obtained 1.17 g (19.90% of theoretical value) of trifluoromethyl pyridine. This substance was found to be a 48:41:11 mixture of α, β and γ isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04172946 |
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| Source dataset | uspto-grants-1979_10 |
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| ORD ID | ord-0cfacf94548244c69efdb199f832c1f8 |
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| Source note | uspto-grants-1979_10 |
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