HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396313Generated: October 27, 2026
2-Amino-5-(trifluoromethyl)pyridine → 2-Chloroamino-5-trifluoromethylpyridine
https://huagongshe.com/reaction/2396313
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-5-(trifluoromethyl)pyridine | HCID 735862 | — |
| Reactant | 2-Chloroamino-3-chloro-5-trifluoromethylpyridine | HCID 18988864 | — |
| Product | 2-Chloroamino-5-trifluoromethylpyridine | HCID 18988854 | — |
Reaction Steps
Then, 16.2 g (0.1 mol) of 2-amino-5-trifluoromethylpyridine was added to the reaction product, and the mixture was heated to 20° C. and stirred at the same temperature for two hours. The reaction product was analyzed by liquid chromatography, whereby 2-chloroamino-3-chloro-5-trifluoromethylpyridine was found to have decreased to 1%, and 2-chloroamino-5-trifluoromethylpyridine was formed afresh in an amount of 31%, and 2-amino-3-chloro-5-trifluoromethylpyridine was formed in an amount of 30%. The rest was the hydrochloride of 2-amino-3-chloro-5-trimethylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05491239 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-904f24d3c6e744ce8b46d5609b8aac5f |
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| Source note | uspto-grants-1996_02 |
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