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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266172Generated: October 26, 2026

Bromoacetonitrile → (4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-acetonitrile

https://huagongshe.com/reaction/2266172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
ReactantSodium hydrideHCID 24758—
Reactant4-Ethyl-7-methyl-benzo[b]thiophen-5-olHCID 59598702—
SolventDimethylformamideHCID 6228—
Product(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-acetonitrileHCID 5959853791.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Ethyl-7-methyl-benzo[b]thiophen-5-ol (438 mg, 2 mmol) was dissolved in 10 ml DMF, and the reaction mixture was cooled to zero degrees C. Sodium hydride (66 mg, 3 mmol) was added and the reaction mixture was stirred 30 minutes at zero C. Bromoacetonitrile (170 ul, 3 mmol) was addeed, and the reaction mixture was stirred 10 minutes at zero degrees C, then allowed to warm to room temperature. The reaction was quenched after 1 hour at room temperature with water, diluted with ethyl acetate, washed with water, brine, and dried over magnesium sulfate. Solvent was removed in vacuo, and the residue chromatographed (10% ethyl acetate in hexanes) to give 422 mg of (4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-acetonitrile as an oil, 80% .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858632B2
Source datasetuspto-grants-2010_12
ORD IDord-758b74ab84c645419d195e3eba3c5e3d
Source noteuspto-grants-2010_12