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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35741Generated: October 26, 2026

Allyl 4-chlorobenzyl ether → 5-{[(4-Chlorophenyl)methoxy]methyl}-3-(4-chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidine

https://huagongshe.com/reaction/35741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl 4-chlorobenzyl etherHCID 15089967—
Reactant1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)-N-methylethanimine N-oxideHCID 72727174—
Product5-{[(4-Chlorophenyl)methoxy]methyl}-3-(4-chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidineHCID 14326451—

Reaction Steps

Derivative 3 (R1 =4-Cl, R2 =CH2C6H4Cl-4 is prepared by a procedure similar to that described in Example 1 by reacting 1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)-N-methylethanimine N-oxide (1: R1 =4-Cl) with allyl 4-chlorobenzyl ether (2: R2 =CH2C6H4Cl-4). The resulting cis-/trans-diastereomeric mixture of the title compound (3: R1 =4-Cl, R2 =CH2C6H4Cl-4) is flash-chromatographed on neutral silica gel using chloroform-methanol (98:2 by volume) as eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767867
Source datasetuspto-grants-1988_08
ORD IDord-7c3ca5ff5259472ca908db97401407ef
Source noteuspto-grants-1988_08