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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847748Generated: October 30, 2026

3-Hydroxybenzyl alcohol → 2-{3-[3-(Hydroxymethyl)phenoxy]propyl}-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/847748

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxybenzyl alcoholHCID 102—
ReactantN-3-BromopropylphthalimideHCID 21611—
ReactantSodium hydrideHCID 24758—
SolventDimethyl SulfoxideHCID 679—
Product2-{3-[3-(Hydroxymethyl)phenoxy]propyl}-1H-isoindole-1,3(2H)-dioneHCID 1278008239.9%

Reaction Steps

A solution of 2.6 g of 3-hydroxybenzyl alcohol in 10 ml of dry dimethylsulfoxide was added dropwise with stirring under ice cooling to a suspension of 0.88 g of 60% sodium hydride in 5 ml of dry dimethylsulfoxide. After the addition, the mixture was stirred at room temperature for 20 minutes, and 6 g of N-bromopropylphthalimide was added. The mixture was reacted at room temperature for 1 hour, and ice water was added. The mixture was extracted with ether, washed with water, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was crystallized with ether to afford 2.6 g of N-[3-[3-(hydroxymethyl)phenoxy]propyl]phthalimide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04293557
Source datasetuspto-grants-1981_10
ORD IDord-27e6a4df3bd14b59972e1291f10c41df
Source noteuspto-grants-1981_10