HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256158Generated: October 27, 2026
Hydrochloric Acid → 2-Chloro-4-hydroxymethyl-3,5,6-trifluoropyridine
https://huagongshe.com/reaction/256158
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | (4-Hydroxymethyl-2,3,5-trifluoropyridin-6-yl)hydrazine | HCID 13985160 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Product | 2-Chloro-4-hydroxymethyl-3,5,6-trifluoropyridine | HCID 13985161 | — |
Reaction Steps
To a solution of 0.35 g (0.0026 mole) of copper (II) chloride in 25 ml of concentrated hydrochloric acid was added slowly at room temperature 0.5 g (0.0026 mole) of (4-hydroxymethyl-2,3,5-trifluoropyridin-6-yl)hydrazine (from Example 6). This mixture was stirred at ambient temperature for two hours and was then refluxed for one hour. After being cooled, the reaction mixture was poured into water and was extracted with diethyl ether. The extract was dried over anhydrous magnesium sulfate, filtered, and the solvent evaporated under reduced pressure, leaving a brown, oily residue. This residue was passed through a short column of silica gel using a hexane/diethyl ether (50/50) mixture as eluant. The appropriate fractions were combined, and the solvent evaporated under reduced pressure, yielding 0.31 g of 2-chloro-4-hydroxymethyl-3,5,6-trifluoropyridine as a yellowish-brown liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04701464 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-76d95ccec31646a5a4ac6509679b3823 |
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| Source note | uspto-grants-1987_10 |
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