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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| Reactant | Methyl 3-methyl-2,3-dihydrobenzofuran-6-carboxylate | HCID 89580905 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Methyl-2,3-dihydro-1-benzofuran-6-carboxylic acid | HCID 89581213 | 78.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051269B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-a8d4dab6b9604fc0aa461d13319553ca |
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| Source note | uspto-grants-2015_06 |
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