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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597860Generated: October 26, 2026

3-Hydroxybenzaldehyde → 3-(2-(1-Pyrrolidinyl)ethoxy)benzaldehyde

https://huagongshe.com/reaction/1597860

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(2-Chloroethyl)pyrrolidine hydrochlorideHCID 81668—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3-(2-(1-Pyrrolidinyl)ethoxy)benzaldehydeHCID 1077524495.6%

Reaction Steps

To a mixture of 3-hydroxybenzaldehyde (4.15 g, 33.98 mmol), KOH (4.93 g) and DMSO (50 ml) was added N-(2-chloroethyl) pyrrolidine hydrochloride (6.94 g). The reaction mixture was stirred at room temperature overnight, then was poured into water (750 ml) and ethyl acetate (350 ml) was added. The layers were separated, the aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with water (2×1000 ml), dried over MgSO4, filtered and stripped to afford 7.12 g of 3-[2-(1-pyrrolidinyl)ethoxy]benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736548
Source datasetuspto-grants-1998_04
ORD IDord-18b4738545ce4be486fd18e50764a7df
Source noteuspto-grants-1998_04