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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896480Generated: October 29, 2026

4-Hydroxybenzaldehyde → 4-(2-Chloroethoxy)benzaldehyde

https://huagongshe.com/reaction/896480

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(2-Chloroethoxy)benzaldehydeHCID 143156—

Reaction Steps

Dissolve 4-hydroxybenzaldehyde (0.082 mol) in dimethylformamide (100 ml) and add potassium carbonate (0.164 mol) and 1-bromo-2-chloroethane (0.246 mol). Stir magnetically for five days at ambient temperature, then hydrolyse the reaction mixture in 500 ml of water and render alkaline with 3 g of sodium hydroxide pellets. Extract twice with 50 ml of ether each time. Dry the organic phase over magnesium sulphate and remove the ether by evaporation under reduced pressure. Purify the resulting oil by flash chromatography using a 9/1 cyclohexane/ether mixture as eluant. Subsequently, remove the mixture of solvents by evaporation under reduced pressure and crystallise the resulting yellow oil and store it in a dessicator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919362B2
Source datasetuspto-grants-2005_07
ORD IDord-9397a16386a74d0fbbdd1942682e041c
Source noteuspto-grants-2005_07