HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901344Generated: October 25, 2026
Sodium Cyanide → 3-(5-Bromobenzo[b]thien-2-yl)-2-(4-methoxyphenyl)butyronitrile
https://huagongshe.com/reaction/1901344
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Toluene ethylacetate | HCID 21584019 | — |
| Reactant | 3-(5-Bromobenzo[b]thien-2-yl)-2-(4-methoxyphenyl)propyl methanesulfonate | HCID 21844314 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-(5-Bromobenzo[b]thien-2-yl)-2-(4-methoxyphenyl)butyronitrile | HCID 21844393 | — |
Reaction Steps
1.2 g of sodium cyanide was dissolved in 30 ml of dimethyl sulfoxide at a temperature of 90° C. To this was gradually added 18.5 g of 3-(5-bromobenzo[b]thien-2-yl)-2-(4-methoxyphenyl)propyl methanesulfonate, followed by stirring at 80° C. for 1 hour. The resulting reaction solution was mixed with an ethyl acetate/toluene mixture, washed with water, and then dried to distill off the solvent. Crystals thus precipitated were washed with ethanol and dried to obtain 5 g of 3-(5-bromobenzo[b]thien-2-yl)-2-(4-methoxyphenyl)butyronitrile. The same compound was also obtained with a yield of 2 g, by concentrating the ethanol solution resulting from the washing of crystals and subjecting the concentrate to silica gel column chromatography using chloroform as an elution solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05576343 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-5813034b79124ce0bfa89e18b52c2a2c |
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| Source note | uspto-grants-1996_11 |
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