HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl 4-chlorobenzyl ether → 5-{[(4-Chlorophenyl)methoxy]methyl}-3-(4-chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl 4-chlorobenzyl ether | HCID 15089967 | — |
| Reactant | 1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)-N-methylethanimine N-oxide | HCID 72727174 | — |
| Product | 5-{[(4-Chlorophenyl)methoxy]methyl}-3-(4-chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04767867 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-7c3ca5ff5259472ca908db97401407ef |
| Source note | uspto-grants-1988_08 |