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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577660Generated: October 27, 2026

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

https://huagongshe.com/reaction/1577660

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+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04288621
Source datasetuspto-grants-1981_09
ORD IDord-eb24da71ec5142e4939e85c053b972e4
Source noteuspto-grants-1981_09