Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481977Generated: October 30, 2026

Water → 5-Bromo-3-cyanomethyl-benzo[B]thiophene

https://huagongshe.com/reaction/481977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
Reactant5-Bromo-3-(bromomethyl)-1-benzothiopheneHCID 21790411—
SolventEthanolHCID 702—
Product5-Bromo-3-cyanomethyl-benzo[B]thiopheneHCID 1775004173.2%

Reaction Steps

A mixture of 0.115 gm (2.34 mMol) sodium cyanide, 2 mL ethanol and 1 mL water was heated to reflux. To this refluxing mixture was added a solution of 0.356 gm (1.16 mMol) 5-bromo-3-(bromomethyl)benzothiophene in 4 mL ethanol. The resulting mixture was heated at reflux for 3 hours. The reaction mixture was cooled to room temperature and then partitioned between water and ethyl acetate. The phases were separated and the aqueous phase extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate and concentrated under reduced pressure. The residue was subjected to flash silica gel chromatography, eluting with hexane containing 10% dichloromethane and 5% ethyl acetate. Fractions containing product were combined and concentrated under reduced pressure to provide 0.214 gm (73%) of the desired nitrile as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05792763
Source datasetuspto-grants-1998_08
ORD IDord-821ce26cf6c34c1a814f2c1a43c2a775
Source noteuspto-grants-1998_08