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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993137Generated: October 29, 2026

Iodoethane → 3,4-Diethoxybenzaldehyde

https://huagongshe.com/reaction/993137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantEthylvanillinHCID 8467—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product3,4-DiethoxybenzaldehydeHCID 7484793.5%

Reaction Steps

3-Ethoxy-4-hydroxy-benzaldehyde (Aldrich, 100 g, 0.602 mole) was dissolved in N,N-dimethylformamide (1 L). The reaction was placed under N2. Solid potassium carbonate (103 g, 0.662 moles) was added and the reaction was stirred 10 minutes. Iodoethane (175 g, 1.26 moles) was added and the reaction was stirred for 16 hours at room temperature. The reaction was monitored by thin-layer chromatography which indicated complete consumption of the phenol to give a new product. The reaction was filtered to remove the potassium carbonate and solvent removed in vacuo. The residue was dissolved in methylene chloride and filtered. Silica gel (200 g) was added and the dichloromethane removed in vacuo. The crude product absorbed on silica gel was submitted to flash chromatography (hexane, 100%, 2 L, then ethyl acetate:hexane, 1:3, 2 L, then ethyl acetate:hexane, 1:1) to yield 109.36 g of 3,4-diethoxy-benzaldehyde 1HNMR (CDCl3): 9.83 (s, 1H), 7.41 (m, 2H), 6.96 (d, 1H), 4.17 (m, 4H), 1.50 (t, 3H) 1.47 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06472393B1
Source datasetuspto-grants-2002_10
ORD IDord-4065ab8444d0470cafc6e8d3c69e18f8
Source noteuspto-grants-2002_10