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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 5-Bromo-3-(bromomethyl)-1-benzothiophene | HCID 21790411 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Bromo-3-cyanomethyl-benzo[B]thiophene | HCID 17750041 | 73.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05792763 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-821ce26cf6c34c1a814f2c1a43c2a775 |
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| Source note | uspto-grants-1998_08 |
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