HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744074Generated: October 30, 2026
2-Hydroxybenzonitrile → HCID 178509671, compound
https://huagongshe.com/reaction/744074
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Hydroxybenzonitrile | HCID 11907 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(2-chloroethyl)-1H-imidazole hydrochloride | HCID 178478570 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178509671 | HCID 178509671 | — |
Reaction Steps
240 mg (60% in oil; 6 mmol) of sodium hydride are added to a solution of 1.43 g (12 mmol) of 2-hydroxybenzonitrile in 10 ml of dimethylformamide. The mixture is stirred at room temperature for 1 hour under nitrogen. 200 mg (1.2 mmol) of 4-(2-chloroethyl)-1H-imidazole hydrochloride and tetrabutylammonium iodide (catalytic amount) are added and the mixture is heated at 80° C. for 3 days. The solvent is evaporated under reduced pressure and the oily residue is stirred in ethanol and filtered. The filtrate is evaporated and the residue subjected to chromatography on a column of silica gel (first eluent chloroform, second eluent 95/5 chloroform/methanol). The title compound is converted to the oxalate and crystallized from an ethanol/diethyl ether (2/1) mixture, M.p.: 170°-171° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05559113 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-a86d5e10324d4d66992c10833b4bbb4f |
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| Source note | uspto-grants-1996_09 |
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