HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356593Generated: October 27, 2026
p-Tolunitrile → 1-(3-Ethoxyphenyl)-2-(4-methylphenyl)-1H-imidazole-4-carboxylic acid
https://huagongshe.com/reaction/2356593
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Tolunitrile | HCID 7724 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-Ethoxyaniline | HCID 12120 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 178466607 | HCID 178466607 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 1-(3-Ethoxyphenyl)-2-(4-methylphenyl)-1H-imidazole-4-carboxylic acid | HCID 59384154 | — |
Reaction Steps
N-(3-Ethoxyphenyl)-4-methylbenzenecarboxamidine To a solution of 2.2 ml (4.4 mmol) of 2.0 M (in tetrahydrofuran) sodium bis(trimethylsilyl)amide in 5.0 mL of tetrahydrofuran at ambient temperature was added 0.52 mL (4.0 mmol) of 3-ethoxyaniline and the resulting solution was stirred for 20 min. To this reaction mixture was slowly added a solution of 0.47 g (4.0 mmol) of p-tolunitrile in 2.0 mL of tetrahydrofuran. The resulting mixture was stirred at ambient temperature for 5 hrs and then poured into brine (25 mL) and dichloromethane (50 mL). The organic layer was separated and the aqueous layer was extracted with dichloromethane (25 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to yield the title compound as yellow solid which was used without further purification. LC/MS 255.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759352B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-76ab3ba3a1034b6b91da825298dc2de0 |
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| Source note | uspto-grants-2010_07 |
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