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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902286Generated: October 31, 2026

Sodium Chloride → 6-Amino-2-pyridinemethanol

https://huagongshe.com/reaction/1902286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantBoraneHCID 6331—
ReactantSodium HydroxideHCID 14798—
Reactant6-Aminopyridine-2-carboxylic acidHCID 351652—
SolventTetrahydrofuranHCID 8028—
Product6-Amino-2-pyridinemethanolHCID 1118260651.2%

Reaction Steps

A mixture of 6-aminopyridine-2-carboxylic acid (5.0 g.) and a 1.35 M solution of borane in tetrahydrofuran (100 ml.) was stirred under argon at reflux for 48 hours. The mixture was cooled and treated with 2 N NaOH (50 ml.) and the mixture stirred at room temperature for 18 hours. The aqueous phase was saturated with sodium chloride and the organic phase separated. The aqueous phase was extracted twice with ethyl acetate and the ethyl acetate extracts combined with the tetrahydrofuran solution and the whole evaporated to dryness. The residue was dissolved in ethyl acetate (100 ml.) and the solution washed with saturated aqueous sodium chloride solution (5 ml.) and then dried and evaporated to dryness to give crude 2-amino-6-hydroxymethylpyridine (2.3 g.) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04362728
Source datasetuspto-grants-1982_12
ORD IDord-e6026faff6f34445a6e3da606b6e7825
Source noteuspto-grants-1982_12