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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078528Generated: October 26, 2026

Ethanol → 1,2-Diethoxy-3-fluorobenzene

https://huagongshe.com/reaction/2078528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl BromideHCID 6332—
ReactantSodium HydroxideHCID 14798—
Reactant2-Ethoxy-3-fluorophenolHCID 54578731—
SolventDichloromethaneHCID 6344—
Product1,2-Diethoxy-3-fluorobenzeneHCID 2246012675%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a 250 ml reactor were added 12.5 (0.08 mol) of 2-ethoxy-3 -fluorophenol [F1], 3.2 g (0.08 mol) of sodium hydroxide and 20 ml of ethanol. After cooling to around 10° C., 20 ml of an ethanol solution of 9.6 g (0.088 ml) of bromoethane was slowly added. After the termination of the addition, they were reacted under a reflux temperature for 3 hours and, after the termination of the reaction, dichloromethane was added, followed by extraction. The extraction liquid was washed with water and dried, and the solvent was removed by distillation to obtain 11.0 g of an oily product [G1]. The process yield was 75%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928268B2
Source datasetuspto-grants-2011_04
ORD IDord-6c12492172ef48cda1f73699d651e1b6
Source noteuspto-grants-2011_04