Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allylbenzene | HCID 9309 | — |
| Reactant | 1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)-N-methylethanimine N-oxide | HCID 72727174 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14426201 | HCID 14426201 | — |
Reaction Steps
A solution of 7.04 g (0.0282 mol) of 1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)-N-methylethanimine N-oxide (1: R1 =4-Cl) [prepared by reacting 2-(1H-imidazol-1-yl)-4'-chloroacetophenone (45.05 g, 0.204 mol), N-methylhydroxylamine hydrochloride (20.93 g, 0.251 mol), and sodium acetate (41.13 g, 0.502 mol) in 550 ml of ethanol] and 3.95 g (0.0334 mol) of allylbenzene (2: R2 =CH2C6H5) in 100 ml toluene is refluxed for 30 hours under a nitrogen atmosphere. Upon cooling to room temperature, the solvent is removed in vacuo. The resulting cis-/trans-diastereomeric mixture of compound 3 (R1 =4-Cl, R2 =CH2C6H5 is flash-chromatographed on neutral silica gel using a 98:2 by volume mixture of chloroform and methanol as eluent to give 3.80 g (36%) of isomer A. Following crystallization from ether a melting point of 118°-120° C. is determined.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04831154 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-6cc232323e1a49b7aa6eb67e6262ad99 |
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| Source note | uspto-grants-1989_05 |
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