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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881364Generated: November 1, 2026

7-Methoxy-2-methyl-4-nitro-1-benzofuran → HCID 11095186, compound

https://huagongshe.com/reaction/1881364

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Methoxy-2-methyl-4-nitro-1-benzofuranHCID 13201901—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 11095186HCID 1109518658.3%

Reaction Steps

7-Methoxy-2-methyl-4-nitro-benzofuran (1.24 g, 6.0 mmol) was hydrogenated using Pd/C (10%, dry, 700 mg) and H2 balloon in EtOH (30 mL) at r.t. for 2 h. The reaction mixture was filtered. Purification of the concentrated filtrate by column chromatography (EtOAc:Hexane=2.5:7.5) afforded 7-methoxy-2-methyl-benzofuran-4-ylamine as a brown oil (620 mg, 58%). 7-Methoxy-2-methyl-benzofuran-4-ylamine (620 mg, 3.5 mmol) was dissolved in CH2Cl2 (10 mL). TCDI (thiocarbodiimidazole, 686 mg, 3.9 mmol) was added to the solution and the reaction mixture was stirred at r.t. for 30 min. Silica gel was added to the reaction mixture and the solvent was removed under vacuum. Purification of the silica gel coated crude product by flash column chromatography (EtOAc:Hexane=2:8) afforded the title product as a pale yellow oil (630 mg, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318790B2
Source datasetuspto-grants-2012_11
ORD IDord-d942229692f94ac88491c0027abc6a1a
Source noteuspto-grants-2012_11