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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287932Generated: October 30, 2026

Sodium Hydroxide → 2-[4-(2-Bromoethoxy)naphthalen-1-yl]-1-benzofuran-3-carboxylic acid

https://huagongshe.com/reaction/1287932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
Reactant1-{2-[4-(2-Bromoethoxy)naphthalen-1-yl]-1-benzofuran-3-yl}ethan-1-oneHCID 21507048—
ReactantSodium BisulfiteHCID 23665763—
ReactantSodium hypobromiteHCID 23673712—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-[4-(2-Bromoethoxy)naphthalen-1-yl]-1-benzofuran-3-carboxylic acidHCID 21507056—

Reaction Steps

A solution of sodium hypobromite, prepared by adding 2.45 g. (0.45 mol.) of bromine to a cooled (0°) solution of 4.5 g. (0.1125 mol.) of sodium hydoxide in 40 ml. of water, was added to a solution of 6.1 g. (0.015 mol.) of 3-acetyl-2-[4-(2-bromoethoxy)naphthyl]benzofuran in 60 ml. of dioxane and the mixture was shaken for 12 hours. Sodium bisulfite was added to the reaction mixture, water was added and the mixture was extracted twice with ether. The aqueous phase was acidified with hydrochloric acid, the resulting precipitate was digested on a steam bath for 1 hour, cooled to 0° and collected by filtration to give 3-carboxy-2-[4-(2-bromo-ethoxy)naphthyl]benzofuran, m.p. 260°-265° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03985896
Source datasetuspto-grants-1976_10
ORD IDord-517b80626db2429f8b30a3a513baeedd
Source noteuspto-grants-1976_10