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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256157Generated: October 29, 2026

Hydrazine hydrate (1:1) → (4-Hydroxymethyl-2,3,5-trifluoropyridin-6-yl)hydrazine

https://huagongshe.com/reaction/256157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant4-Hydroxymethyl-2,3,5,6-tetrafluoropyridineHCID 13985158—
SolventEthanolHCID 702—
Product(4-Hydroxymethyl-2,3,5-trifluoropyridin-6-yl)hydrazineHCID 13985160—

Reaction Steps

To a solution of 1.0 g (0.0055 mole) of 4-hydroxymethyl-2,3,5,6-tetrafluoropyridine (from Example 5) in 50 ml of ethanol was added 0.2 g (0.004 mole) of hydrazine hydrate. This mixture was stirred for approximately twenty-four hours during which a white precipitate formed. The reaction mixture was filtered, and the filtrate was concentrated by evaporating the solvent under reduced pressure. Water and ether were added to this residue. The ether layer was separated, dried, and the solvent evaporated, leaving a yellow solid, (4-hydroxymethyl-2,3,5-trifluoropyridin-6-yl)hydrazine. The structure and nmr data are set forth in Table 1C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04701464
Source datasetuspto-grants-1987_10
ORD IDord-25a321ef0f42488e9da23e3b79057915
Source noteuspto-grants-1987_10