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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 487241Erstellt: 25. Oktober 2026

Dichloromethane → N-ethoxycarbonylmethylthioethyl-N-n-butylcinnamamide

https://huagongshe.com/reaction/487241

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt3-(3,5-Ditert-butyl-4-hydroxyphenyl)prop-2-enoic acidHCID 99819—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktN-ethoxycarbonylmethylthioethyl-n-butylamineHCID 86747655—
LösungsmittelWaterHCID 962—
ProduktN-ethoxycarbonylmethylthioethyl-N-n-butylcinnamamideHCID 67822768105%

Reaktionsschritte

First, 5.53 g of 3,5-di-t-butyl-4-hydroxycinnamic acid, 4.4 g of N-ethoxycarbonylmethylthioethyl-n-butylamine, and 4.0 g of 1-ethyl-3-(3dimethylaminopropyl)carbodiimide hydrochloride (WSC) were added to 100 ml of dichloromethane and the mixture was agitated for 3 hours at room temperature. Then, this reaction mixture was poured into water, and after chloroform extraction the chloroform layer was dehydrated with anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The residue so obtained was separated and purified by column chromatography on silica gel with chloroform, after which hexane was added and crystallization yielded 7.34 g of an N-ethoxycarbonylmethylthioethyl-N-n-butylcinnamamide derivative (yield 79.5%) in the form of white crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05294643
Quelldatensatzuspto-grants-1994_03
ORD IDord-cfc51979bbf84a81b826fb784ea1f31d
Quellennotizuspto-grants-1994_03