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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2394324Erstellt: 25. Oktober 2026

Water → N1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxycarbonyl-L-valinamide

https://huagongshe.com/reaction/2394324

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-MethylmorpholineHCID 7972—
EduktPhenyl thioxochloroformateHCID 70498—
EduktN1-[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamideHCID 22866848—
LösungsmittelDichloromethaneHCID 6344—
ProduktN1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxycarbonyl-L-valinamideHCID 5371342076,7%

Reaktionsschritte

0.4 g of N-methylmorpholine was added to a suspension containing 1.1 g of N1 -[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide suspended in 40 ml of methylene chloride, at -15° C. After 0.7 g of phenyl chlorothionoformate was added to the mixture at -15° C., the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred, and then the whole mixture was stirred for 15 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed with water, the organic layer was dried over anhydrous magnesium sulfate and the methylene chloride was removed under reduced pressure. The residue was purified by column chromatography on silica gel, thus yielding 1.2 g of the desired product in the form of a yellow glutinous substance (yield: 75%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05811424
Quelldatensatzuspto-grants-1998_09
ORD IDord-d3459f31632b4562aafcf48ee493a05f
Quellennotizuspto-grants-1998_09