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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234140Generated: October 31, 2026

Sodium hydride → 5-(t-Butoxycarbonylmethyl)oxy-2-hydroxymethylpyridine

https://huagongshe.com/reaction/234140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant5-Hydroxy-2-hydroxymethylpyridineHCID 419490—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-(t-Butoxycarbonylmethyl)oxy-2-hydroxymethylpyridineHCID 2146605185%

Reaction Steps

The solution of 5-hydroxy-2-hydroxymethylpyridine (5.0 g) in DMF (10 ml) was titrated under ice-cooling in the suspension of sodium hydride (60% purity, 1.6 g) in DMF (10 ml). After 10 minutes, the mixture was heated to room temperature and stirred for 15 minutes. After t-butyl bromoacetate (6 ml) was added to the mixture under ice-cooling, the resulting mixture was stirred under ice-cooling for 10 minutes and at room temperature for 45 minutes. The reaction mixture was diluted with ethyl acetate, washed with water and brine and dried over anhydrous magnesium sulfate. After the solvents were removed by distillation, the residue was purified by column chromatography on silica gel with an eluent system of chloroform→chloroform: methanol=50:1 to give 8.16 g of 5-(t-butoxycarbonylmethyl)oxy-2-hydroxymethylpyridine (yield, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594004
Source datasetuspto-grants-1997_01
ORD IDord-4ae1f98634054382bc41edef27873657
Source noteuspto-grants-1997_01