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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345927Generated: November 1, 2026

3-Hydroxybenzyl alcohol → 2-[3-(Hydroxymethyl)phenoxy]acetonitrile

https://huagongshe.com/reaction/345927

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxybenzyl alcoholHCID 102—
ReactantPotassium CarbonateHCID 11430—
ReactantBromoacetonitrileHCID 11534—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
Product2-[3-(Hydroxymethyl)phenoxy]acetonitrileHCID 11321137—

Reaction Steps

A mixture of 3-hydroxymethyl phenol (0.081 mol), bromacetonitrile (0.081 mol) and anhydrous potassium carbonate (0.081 mol) in acetone (160 ml) and dimethylformamide (20 ml) are heated at reflux for 48 hrs. The reaction mixture is filtered and evaporated. The residue is diluted with ethyl acetate (150 ml), washed with 10% aqueous sodium hydroxide solution (3×100 ml) and then with brine (3×100 ml). The ethyl acetate solution is dried (magnesium sulfate) and chromatographed using a silica gel column (ca. 100 g) and eluted with 1:1 petroleum ether: ethylacetate (2l). The resultant oil is used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05059610
Source datasetuspto-grants-1991_10
ORD IDord-c6eb6e11b5604bdcb7ffb3896196aa55
Source noteuspto-grants-1991_10