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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364732Generated: November 1, 2026

Methyl 2-methyl-7-nitro-2,3-dihydrobenzofuran-4-carboxylate → Methyl 7-amino-2-methyl-2,3-dihydrobenzofuran-4-carboxylate

https://huagongshe.com/reaction/2364732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-methyl-7-nitro-2,3-dihydrobenzofuran-4-carboxylateHCID 68107419—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 7-amino-2-methyl-2,3-dihydrobenzofuran-4-carboxylateHCID 6810784691.9%

Reaction Steps

Methyl 2-methyl-7-nitro-2,3-dihydrobenzofuran-4-carboxylate 30a (100 mg, 0.42 mmol) was dissolved in 20 mL of methanol followed by the addition of palladium/carbon (10 mg, 10%), filled with hydrogen for three times. The reaction solution was stirred for 12 hours and filtered. The filtrate was concentrated under reduced pressure to obtain the title compound methyl 7-amino-2-methyl-2,3-dihydrobenzofuran-4-carboxylate 30b (80 mg, yield: 91.0%) as a colorless oil liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-650d439649754ea690b74b723fcf9474
Source noteuspto-grants-2014_04