HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591074Generated: October 31, 2026
Imidazole → 5-(1H-imidazol-1-yl)-7,8-dihydronaphthalene-2-carbonitrile
https://huagongshe.com/reaction/1591074
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Oxo-5,6,7,8-tetrahydronaphthalene-2-carbonitrile | HCID 10899132 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(1H-imidazol-1-yl)-7,8-dihydronaphthalene-2-carbonitrile | HCID 9837392 | — |
Reaction Steps
175 μl of thionyl chloride are added dropwise to a solution of 272 mg of imidazole in 2.5 ml of methylene chloride. 342 mg of 6-cyano-1-tetralone are added in portions to the resulting white suspension, and the reaction mixture is stirred for 7 hours at 40° and then for 24 hours at room temperature. 386 mg of potassium carbonate in 1.6 ml of water are added to the reaction mixture, which is then extracted with chloroform. After drying the organic phase over sodium sulfate, concentration is carried out under reduced pressure. The resulting crude product is purified by column chromatography (0.04-0.063 mesh SIO2, hexane/ethyl acetate 1:2). Crystallisation from ether yields the title compound in the form of colourless crystals; m.p. 152°-153°. TLC (ethyl acetate): Rf=0.17.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05206256 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-fcd1697a45a348e9ba48221609987dbe |
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| Source note | uspto-grants-1993_04 |
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