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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170488Generated: October 29, 2026

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

https://huagongshe.com/reaction/2170488

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 numberUS09051269B2
Source datasetuspto-grants-2015_06
ORD IDord-a8d4dab6b9604fc0aa461d13319553ca
Source noteuspto-grants-2015_06