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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363100Generated: November 1, 2026

Potassium Carbonate → 4-(2-Chlorobenzyloxy)-3,5-dichlorophenoxyacetaldehyde diethyl acetal

https://huagongshe.com/reaction/363100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
Reactant4-(2-Chlorobenzyloxy)-3,5-dichlorophenolHCID 54095899—
SolventDimethylformamideHCID 6228—
Product4-(2-Chlorobenzyloxy)-3,5-dichlorophenoxyacetaldehyde diethyl acetalHCID 5407523272%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 0.85 g of 4-(2-chlorobenzyloxy)-3,5-dichlorophenol, 0.47 ml of bromoacetaldehyde diethyl acetal, 0.46 g of potassium carbonate and 20 ml of N,N-dimethylformamide was stirred at 90° C. for 6 hours. After cooling to room temperature, the reaction mixture was poured into ice water, and extracted twice with 50 ml of diethyl ether. The combined ether layer was washed with water, and dried with anhydrous magnesium sulfate, followed by removal of the solvent by distillation under reduced pressure. The residue was subjected to silica gel chromatography, which afforded 0.85 g of 4-(2-chlorobenzyloxy)-3,5-dichlorophenoxyacetaldehyde diethyl acetal (72% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872137
Source datasetuspto-grants-1999_02
ORD IDord-6300e521e43f44889713381f2ba869df
Source noteuspto-grants-1999_02