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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747053Generated: November 1, 2026

4-Hydroxybenzyl Alcohol → HCID 59478957, compound

https://huagongshe.com/reaction/1747053

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzyl AlcoholHCID 125—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium AzideHCID 33557—
Reactanttert-Butyl bromoacetateHCID 79177—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59478957HCID 59478957—

Reaction Steps

To a mixture of 2.97 g of 4-(hydroxymethyl)phenol, 4.90 g of tert-butyl bromoacetate, and 25 ml of DMF was added 4.96 g of potassium carbonate at room temperature, followed by stirring for 12 hours. To the reaction solution was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was then evaporated. The residue was purified by silica gel column chromatography (eluent: ethyl acetate-hexane) to obtain a pale yellow oily substance. This oily substance was subjected to methanesulfonylation in accordance with Production Example 15, and then reacted with sodium azide to obtain 4.03 g of tert-butyl[4-(azidomethyl)phenoxy]acetate as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150541B2
Source datasetuspto-grants-2015_10
ORD IDord-2081405710934da59bb751078eb2bc47
Source noteuspto-grants-2015_10