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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364661Generated: November 1, 2026

Methyl 7-nitrobenzofuran-4-carboxylate → Methyl 7-amino-2,3-dihydrobenzofuran-4-carboxylate

https://huagongshe.com/reaction/2364661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 7-nitrobenzofuran-4-carboxylateHCID 20738655—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 7-amino-2,3-dihydrobenzofuran-4-carboxylateHCID 6810768662.4%

Reaction Steps

Methyl 7-nitrobenzofuran-4-carboxylate 1f (820 mg, 3.70 mmol) was dissolved in 150 mL of methanol in an ice-water bath, added with (164 mg, 10%) palladium/carbon, methanol (0.3 mL). The resulting solution was subjected to hydrogenation for 16 hours at 3 atmosphere at room temperature. The resulting mixture was filtered and washed with 50 mL of methanol, concentrated under reduced pressure. The crude residue was recrystallised by the mixture solvent of 25 mL ethyl acetate and n-hexane (V/V=1:4) to obtain the title compound methyl 7-amino-2,3-dihydrobenzofuran-4-carboxylate 1g (446 mg, yield: 62.0%) as a gray solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-2d982ef75d1a4446a41cb0a5153faed8
Source noteuspto-grants-2014_04