Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Reactant | HCID 14514396 | HCID 14514396 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | 1-Methylpyrrolidine | HCID 8454 | — |
| Product | HCID 14514397 | HCID 14514397 | 30.8% |
Reaction Steps
0.04 g of bromine compound (of example 1) is dissolved in 2 ml of N- methylpyrrolidine, 0.05 g of copper(I) cyanide is added and stirred under argon for 5 hours at 180° C. Ammonia water is added to the reaction solution and then extracted with ethyl acetate. The organic phase is concentrated by evaporation in a vacuum and the remaining oil is distilled on a bulb tube, boiling point 180° C./0.03 mbar. 0.01 g of 5-[1-(1-imidazolyl)-butyl]thiophene-2-carbonitrile is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05021434 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-08163908a69c4e96a00fd0572e65d1ff |
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| Source note | uspto-grants-1991_06 |
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