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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762280Generated: October 26, 2026

Allylbenzene → HCID 14426201, compound

https://huagongshe.com/reaction/1762280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylbenzeneHCID 9309—
Reactant1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)-N-methylethanimine N-oxideHCID 72727174—
SolventTolueneHCID 1140—
ProductHCID 14426201HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831154
Source datasetuspto-grants-1989_05
ORD IDord-6cc232323e1a49b7aa6eb67e6262ad99
Source noteuspto-grants-1989_05