Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 22996179 | HCID 22996179 | — |
| Product | HCID 22996246 | HCID 22996246 | — |
Reaction Steps
Hydrogen chloride gas was passed through a solution of 5-ethoxymethyl-2-methoxy-benzonitrile (181 mg, 0.947 mmol) in anhydrous ethanol (30 mL) at room temperature. After 2 h, hydrogen chloride gas was stopped and the reaction vessel was sealed. After stirring at room temperature for 12 h, the reaction vessel was cooled to 0° C. and opened. The solvent was evaporated in vacuo to dryness to afford crude ethyl 5-ethoxymethyl-2-methoxy-benzimidate hydrochloride. meso-1,2-Bis-(4-chloro-phenyl)-ethane-1,2-diamine (253 mg, 0.9 mmol), triethylamine (186 μL, 1.5 mmol) and ethanol (10 mL) were added and the resulting mixture was heated at reflux for 12 h. The solvent was removed and the residue was taken up in methylene chloride (2 mL) and sodium bicarbonate solution (2 mL). The product was extracted with methylene chloride (2×30 mL). The organic layers were washed with brine (1×5 mL) and dried over anhydrous sodium sulfate. The solid was then filtered off, and the filtrate was concentrated in vacuo. The residue was purified by flash chromatography (Biotage system, KP-Sil™ 32-63 μm, 60 Å silica gel) eluting with 70-100% ethyl acetate in hexanes to afford 4,5-bis-(4-chloro-phenyl)-2-(5-ethoxymethyl-2-methoxy-phenyl)-4,5-dihydro-1H-imidazole (136 mg, 33%). LR-MS (APCI): 455 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06617346B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-92c5aa2c6221435aa67af8d5cccca6c6 |
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| Source note | uspto-grants-2003_09 |
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