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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181671Generated: October 31, 2026

Sodium Carbonate → Methyl 3-methyl-1-benzofuran-6-carboxylate

https://huagongshe.com/reaction/2181671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium FormateHCID 2723810—
ReactantMethyl 3-(allyloxy)-4-iodobenzoateHCID 22481791—
Catalystpalladium(II) acetateHCID 167845—
CatalystTetrabutylammonium chloride hydrateHCID 16212273—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-methyl-1-benzofuran-6-carboxylateHCID 2248175267%

Reaction Conditions

Temperature80 °C

Reaction Steps

Methyl 3-(allyloxy)-4-iodobenzoate (2.0 g, 6.28 mmol) is dissolved in DMF (15 ml), treated with Pd(OAc)2 (71 mg, 0.31 mmol), Na2CO3 (1.67 g, 15.7 mmol), sodium formate (427 mg, 6.28 mmol), and n-Bu4NCl.H2O (1.92 g, 6.92 mmol) and stirred at 80° C. for 2 days. The mixture is then filtered, the liquor is diluted with EtOAc (75 ml) and washed with 50% saturated NaCl (4×25 ml) followed by 5% HCl (25 ml). The organic layer is dried (Na2SO4), filtered, and concentrated to a brown oil. The crude material is chromatographed over 50 g slurry-packed silica gel, eluting with 20% EtOAc/hexane. The appropriate fractions are combined and concentrated to afford 797 mg (67%) of methyl 3-methyl-1-benzofuran-6-carboxylate as a pale oil. HRMS (FAB) calcd for C11H10O3+H: 191.0708, found 191.0714 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894042B2
Source datasetuspto-grants-2005_05
ORD IDord-aad4a5cd9e014d83a0ae4bdefd50e538
Source noteuspto-grants-2005_05