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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 126976Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/126976

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt1-(Bromomethyl)-3-phenoxybenzeneHCID 94544—
Edukt2-(4-Chlorophenyl)-3-methylbutanamideHCID 12898176—
KatalysatorSilver tetrafluoroborateHCID 159722—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3-Phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanimidateHCID 12898177—

Reaktionsschritte

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+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04254264
Quelldatensatzuspto-grants-1981_03
ORD IDord-2e3a9f3858cd4cdd9377665e6ee2c8c1
Quellennotizuspto-grants-1981_03