Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2,6-Dichloro-3-(trifluoromethyl)pyridine | HCID 1810337 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13064152 | HCID 13064152 | — |
| Product | 6-Chloro-5-(trifluoromethyl)pyridin-2-amine | HCID 13064153 | — |
Reaction Steps
6.48 g of 2,6-dichloro-3-trifluoromethylpyridine and 18 ml of 28% aqueous ammonia were placed in a 50 ml autoclave, and the mixture was reacted for 24 hours at 90° C. (inner pressure: about 2 atms.). After completion of the reaction, the reaction product was allowed to cool, and methylene chloride was added thereto to thereby extract the desired product and the unreacted starting material. The methylene chloride in the extract was evaporated off, and the separation was carried out by silica gel column chromatography using firstly n-hexane and then methylene chloride as eluents. Thus, 1.12 g of 2-amino-3-trifluoromethyl-6-chloropyridine having a melting point of 99° to 101° C. and 1.37 g of 2-amino-5-trifluoromethyl-6-chloropyridine having a melting point of 111° to 113° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04349681 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-d15dd128107740b0911292a0e20b63a8 |
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| Source note | uspto-grants-1982_09 |
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