HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52133Generated: October 26, 2026
Triethylamine → 3-Diethylthiocarbamoyloxy-2-fluoropyridine
https://huagongshe.com/reaction/52133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethylthiocarbamoyl chloride | HCID 66607 | — |
| Reactant | 2-Fluoro-3-hydroxypyridine | HCID 2762785 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Diethylthiocarbamoyloxy-2-fluoropyridine | HCID 19963242 | 86.5% |
Reaction Steps
36.2 g (358 mmol) of triethylamine and 54.3 g (358 mmol) of diethylthiocarbamoyl chloride are added in succession to a suspension of 36.7 g (325 mmol) of 2-fluoro-3-hydroxypyridine in 150 ml of toluene at room temperature, and the reaction mixture is heated at 75° C. After the reaction mixture has been stirred at this temperature for 1 hour, it is cooled to room temperature, diluted with ethyl acetate, washed 3 times with water, dried over Na2SO4 and concentrated in vacuo at 60° C.; 80 g of brown oil which, after recrystallization from Et2O/hexane, gave 64.2 g (86%) of brown crystals of m.p. 52°-54° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616590 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-685f9a15481e484ea0fd2be8b7a312fa |
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| Source note | uspto-grants-1997_04 |
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