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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894950Generated: October 25, 2026

Dichloromethane → 3-Phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanimidate

https://huagongshe.com/reaction/894950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-(Bromomethyl)-3-phenoxybenzeneHCID 94544—
Reactant2-(4-Chlorophenyl)-3-methylbutanamideHCID 12898176—
CatalystSilver tetrafluoroborateHCID 159722—
SolventDiethyl EtherHCID 3283—
Product3-Phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanimidateHCID 12898177—

Reaction Steps

To a refluxing solution of 2.72 g (12.9 mmol) of 2-(4-chlorophenyl)-3-methylbutyramide and 2.27 g (8.6 mmol) of 3-phenoxybenzyl bromide in a solution of 15 ml dichloromethane and 3 ml ethyl ether is added a solution of 1.83 g (9.5 mmol) of silver tetrafluoroborate in ether. The mixture is refluxed for 2 hours and then separated by pouring into ice cold aqueous ethyl acetate/sodium bicarbonate. The organic phase is washed with water, dried and stripped of solvent. The residue is triturated with ether and filtered. The filtrate is concentrated and chromatographed on silica gel, eluting with 25% ethyl acetate/-hexane, and then on plates using 35% ethyl acetate/hexane, to yield 3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanimidate, MS m/e 393 (M-hu +(M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04285879
Source datasetuspto-grants-1981_08
ORD IDord-63ef7c904ad547c69f6fe9cf27a5a4f1
Source noteuspto-grants-1981_08