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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565185Generated: October 29, 2026

Acetone → 2,5-Diethoxybenzaldehyde

https://huagongshe.com/reaction/565185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 131722258HCID 131722258—
Product2,5-DiethoxybenzaldehydeHCID 3434314—

Reaction Steps

A suspension of 9.66 g (70 mmol) 2,5-dihydroxybenzaldehyde N2, 32.75 g (210 mmol) iodoethane, 24.19 g (175 mmol) K2CO3 in 350 ml acetone was heated to reflux for 18 hours under nitrogen. The solvent was evaporated and the residue was dissolved in 300 ml CHCl3 and 300 ml water. The organic phase was washed with 2×300 ml 2.5% Na2CO3 and 300 ml saturated NaCl and dried over Na2SO4. The solvent was evaporated and the residue (13.5 g) purified with a silica gel column (silica gel 100, CHCl3/cyclohexane: 1/1, v/v), affording 8.61 g light yellow oil, which crystallized after cooling to room temperature (yield. 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06171866B2
Source datasetuspto-grants-2001_01
ORD IDord-43be5279e9e04366bc268cabc1c361b6
Source noteuspto-grants-2001_01