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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766285Generated: November 1, 2026

3-methyl-5-nitro-1-benzothiophene → HCID 20824576, compound

https://huagongshe.com/reaction/1766285

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-methyl-5-nitro-1-benzothiopheneHCID 268625—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 20824576HCID 2082457639%

Reaction Steps

To a solution of 3-methyl-5-nitro-benzo[b]thiophene [18] (95 mg, 0.492 mmol) in methanol (20 mL) was added 5% palladium on carbon (20 mg) and the mixture was stirred under 1 atm H2 for 8.5h. The mixture was filtered through celite and the filtrate evaporated. The residue was passed through a silica plug to afford 3-methyl-benzo[b]thiophen-5-ylamine as a dark orange solid (31 mg, 39%), single spot at Rf 0.31 (4:1 hexane:ethyl acetate). 1H NMR (CDCl3): δ 7.60 (1H, d, J=8.4 Hz), 7.02 (1H, s), 7.00 (1H, d, J=2.2 Hz), 6.79 (1H, dd, J=8.4, 2.2 Hz), 2.37 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230020B2
Source datasetuspto-grants-2007_06
ORD IDord-b9d4928ef6074456bfc8c703fa023de4
Source noteuspto-grants-2007_06