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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181650Generated: October 26, 2026

Methane → 1-Benzofuran-6-carboxylic acid

https://huagongshe.com/reaction/2181650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-hydroxy-4-[2-(trimethylsilyl)ethynyl]benzoateHCID 22481756—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventEtOH triethylamineHCID 22663003—
Product1-Benzofuran-6-carboxylic acidHCID 1786723493.3%

Reaction Conditions

Temperature75 °C

Reaction Steps

Methyl 3-hydroxy-4-[(trimethylsilyl)ethynyl]benzoate (3.0 g, 12.1 mmol) is dissolved in 1:1 EtOH/Et3N (30 mL), is treated with CuI (114 mg, 0.6 mmol), and the reaction is warmed to 75° C. for 3 h. The mixture is treated with DARCO and MeOH (15 mL) and heated to reflux for 1 h. The reaction is filtered through a fine fritted-glass funnel, the filtrate is treated with 3N NaOH (24.2 ml, 72.5 mmol), and the mixture is stirred overnight at RT. The mixture is concentrated to dryness, the residue is dissolved in H2O (20 mL), and the pH of the mixture is adjusted to 2 with 12N HCl. The resulting yellow precipitate is collected, washed with water, and is dried to give 1.83 g (93%) of benzofuran-6-carboxylic acid as a tan solid. HRMS (FAB) calcd for C9H6O3+H: 163.0395, found 163.0389 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894042B2
Source datasetuspto-grants-2005_05
ORD IDord-b05f5983b46946729961f375a5895c4d
Source noteuspto-grants-2005_05