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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181646Generated: October 31, 2026

Methyl 1-benzofuran-5-carboxylate → 1-Benzofuran-5-Carboxylic Acid

https://huagongshe.com/reaction/2181646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 1-benzofuran-5-carboxylateHCID 12674941—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
Product1-Benzofuran-5-Carboxylic AcidHCID 595656100.3%

Reaction Conditions

Temperature65 °C

Reaction Steps

A stirred mixture of methyl benzofuran-5-carboxylate (1.3 g, 7.38 mmol) in MeOH (51 mL) and sodium hydroxide (41 mL of a 5% aqueous solution) is heated to 65° C. for 4 h. The mixture is cooled to rt, and MeOH is removed in vacuo. The remaining aqueous layer is extracted with CH2Cl2. The CH2Cl2 layer is discarded, and the aqueous layer is acidified to pH=1 with concentrated hydrochloric acid. The aqueous layer is extracted with CHCl3. The organic layer is washed with water, dried (MgSO4), filtered and concentrated in vacuo to afford 1.2 g (98%) of benzofuran-5-carboxylic acid as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 12.9, 8.30, 8.11, 7.92, 7.69, 7.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894042B2
Source datasetuspto-grants-2005_05
ORD IDord-f3d97d2bfe95416cb6771756392a4b84
Source noteuspto-grants-2005_05