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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450474Generated: October 31, 2026

5-Bromo-3-methyl-1-benzothiophene → 3-Methyl-1-benzothiophene-5-carbonitrile

https://huagongshe.com/reaction/1450474

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-3-methyl-1-benzothiopheneHCID 14175764—
ReactantHCID 178418546HCID 178418546—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-Methyl-1-benzothiophene-5-carbonitrileHCID 2326173290.1%

Reaction Steps

To copper (I) cyanide (0.569 g, 6.35 mmol) was added 5-bromo-3-methyl benzo[b]thiophene (1.179 g, 5.19 mmol) in N-methylpyrrolidinone (10 ml) and the mixture was stirred at 180°-90° C. for 17 h. This was then partitioned between ether (75 ml) and ammonia solution (75 ml). The ether layer was separated, washed with more ammonia solution (2×50 ml), dried (Na2SO4) and evaporated in vacuo to leave 0.81 g of an off-white solid. Chromatography on flash silica, eluting with 10% ethyl acetate/petroleum ether yielded 0.76 g (85%) of the title compound as a white solid. δ (CDCl3) 2.47 (3H, s), 7.23 (1H, s), 7.55 (1H, dd, J=8.3 and 1.5 Hz), 7.93 (1H, d, J=8.4 Hz), 8.03 (1H, d, J=1.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602162
Source datasetuspto-grants-1997_02
ORD IDord-57860e4a6c9841baa4dd26c52335a251
Source noteuspto-grants-1997_02