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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525159Generated: October 30, 2026

Sodium Hydroxide → 5-Chloro-7-methyl-1-benzofuran

https://huagongshe.com/reaction/525159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium AcetateHCID 517045—
Reactant[(4-chloro-2-formyl-6-methylphenyl)oxy]acetic AcidHCID 86674828—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventAcetic AnhydrideHCID 7918—
Product5-Chloro-7-methyl-1-benzofuranHCID 5972625215.4%

Reaction Steps

A solution of [(4-chloro-2-formyl-6-methylphenyl)oxy]acetic acid (4.69 mmol) in acetic anhydride (20 mL) was treated with sodium acetate (14.07 mmol). The resulting solution was heated to reflux and stirred for three days. The brown reaction solution was allowed to cool to room temperature, and was diluted with toluene (10 mL). The solution was then treated with 1N aq NaOH (10 mL) and was stirred at room temperature for 20 min. The solution was then further diluted with water (50 mL) and was extracted using ethyl acetate. The combined organic layers were dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting brown residue was purified by flash chromatography (hexanes) to provide the title compound as a clear oil (120 mg, 15% yield). 1H NMR (400 MHz, DMSO-d6) ppm 8.07 (d, J=2.27 Hz, 1H) 7.55 (d, J=1.77 Hz, 1H) 7.20 (d, J=1.01 Hz, 1H) 6.94 (d, J=2.27 Hz, 1H) 2.47 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340529B2
Source datasetuspto-grants-2016_05
ORD IDord-304dc9b9e5ea4cbb80c61bf52bb7240f
Source noteuspto-grants-2016_05