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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479748Generated: October 31, 2026

Triethylamine → 3-Methyl-2,3-dihydro-1-benzofuran-6-carboxylic acid

https://huagongshe.com/reaction/1479748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantMethyl 3-methyl-2,3-dihydrobenzofuran-6-carboxylateHCID 89580905—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
Product3-Methyl-2,3-dihydro-1-benzofuran-6-carboxylic acidHCID 8958121378.6%

Reaction Steps

To a reversible vial was added methyl 3-methyl-2,3-dihydrobenzofuran-6-carboxylate (384 mg, 2 mmol) in methanol (16 mL) was added triethylamine (900 mg, 9 mmol), palladium acetate (116 mg, 0.5 mmol) and 1,3-bis(diphenylphosphino) propane (480 mg, 1 mmol). Then the reaction mixture was charged with carbonate monoxide under 15 atm at 110° C. for 12 hours. The suspension was concentrated in vacuum and quenched with aqueous 1N hydrochloric acid (5 mL). The residue was taken up with water (50 mL) and extracted with dichloromethane (50 mL). The combined extract was dried over sodium sulphate, evaporated and purified by column chromatography (silica gel, dichloromethane/methanol=20:1) to give the product 3-methyl-2,3-dihydrobenzofuran-6-carboxylic acid (0.28 g, 78%) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409865B2
Source datasetuspto-grants-2016_08
ORD IDord-4a52870504ba46ba96f2fe5cf743e778
Source noteuspto-grants-2016_08