HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2094487Generated: October 30, 2026
Thionyl Chloride → 3-Ethyl isonicotinic acid chloride
https://huagongshe.com/reaction/2094487
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Ethylisonicotinic acid | HCID 45084743 | — |
| Product | 3-Ethyl isonicotinic acid chloride | HCID 87189137 | — |
Reaction Steps
A mixture of 0.62 g of 3-ethyl isonicotinic acid 4 ml of thionyl chloride was heated to reflux for 2.5 hours. The reaction mixture was cooled to room temperature, the reaction mixture was concentrated under reduced pressure to give 3-ethyl isonicotinic acid chloride. A mixture of the resultant 3-ethyl isonicotinic acid chloride and 3 ml of DMF was added dropwise to a mixture of 0.87 g of 2-amino-5-chloro-4-trifluoromethylphenol, 0.83 g of triethylamine and 3 ml of DMF while ice-cooling. The reaction mixture was stirred at room temperature for two hours, and then water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with water and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.23 g of N-[4-chloro-2-hydroxy-5-(trifluoromethyl)phenyl]-3-ethyl isonicotinamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445522B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-7e834041865c4d97b5d276f194549e9d |
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| Source note | uspto-grants-2013_05 |
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