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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264706Erstellt: 24. Oktober 2026

Sodium Hydroxide → N-{5-(4-Chlorophenyl)pent-1-en-4-yl}-N-ethoxymethyl-3,5-dimethylbenzamide

https://huagongshe.com/de/reaction/264706

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktChloromethyl ethyl etherHCID 18523—
EduktN-{5-(4-chlorophenyl)pent-1-en-4-yl}-3.5-dimethylbenzamideHCID 19035936—
KatalysatorBenzyltributylammonium chlorideHCID 159952—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-{5-(4-Chlorophenyl)pent-1-en-4-yl}-N-ethoxymethyl-3,5-dimethylbenzamideHCID 19035912—

Reaktionsschritte

2.36 ml (25.2 mmol) of chloromethyl ethyl ether are added in small portions over the course of 2 hours to a vigorously stirred solution of 5.5 g (16.8 mmol) of N-{5-(4-chlorophenyl)pent-1-en-4-yl}-3.5-dimethylbenzamide and 100 mg of benzyltributylammonium chloride in 15 ml of 50% strength aqueous sodium hydroxide solution and 15 ml of dichloromethane at 0°-5°. The organic phase is taken up in dichloromethane and water, the organic phase is separated off, dried over sodium sulfate and evaporated to dryness under reduced pressure. The oily residue is purified by chromatography on silica gel with ethyl acetate/hexane (1:4) as mobile phase; TLC (ethyl acetate/hexane; 1:3):Rf =0.50; 1H-NMR (300 MHz, CDCl3):mixture of rotamers, δ=7.31-7.18 (m, 4 H), 7.04-6.85 (m, 2.6 H), 6.42 (hr. s, 0.4 H), 5.92-5.60 (m, 1 H), 5.20-5.02 (m, 2 H), 4.54-4.24 (m, 2 H), 3.96-3.67 (m, 1 H), 3.25-2.40 (m, 6 H), 2.28 (s, ca 5 H), 2.24 (s, ca 1 H), 1.34-1.21(m, ca 0.5 H), 1.08 (t, J=7, ca 2.5 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05646144
Quelldatensatzuspto-grants-1997_07
ORD IDord-fdce7d4e72c04bffb1204638a1122797
Quellennotizuspto-grants-1997_07