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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1242543Erstellt: 25. Oktober 2026

Pyridine → (2S,4EZ)-4-[(allyloxy)imino)-1-(tert-butoxycarbonyl)-2-pyrrolidinecarboxylic acid

https://huagongshe.com/reaction/1242543

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt(2S)-1-(tert-butoxycarbonyl)-4-oxopyrrolidine-2-carboxylic acidHCID 11593804—
EduktO-Prop-2-en-1-ylhydroxylamine--hydrogen chloride--water (1/1/1)HCID 16211718—
LösungsmittelEthanolHCID 702—
Produkt(2S,4EZ)-4-[(allyloxy)imino)-1-(tert-butoxycarbonyl)-2-pyrrolidinecarboxylic acidHCID 5871456294,3%

Reaktionsschritte

A solution was made containing (2S)-1-(tert-butoxycarbonyl)-4-oxo-2-pyrrolidinecarboxylic acid (Intermediate 1, 5.0 g, 22 mmol) and O-allylhydroxylamine hydrochloride monohydrate (7.2 g, 65.5 mmol) in a 1:1 mixture of pyridine and ethanol (100 ml). The reaction was heated to reflux for 2.5 h before cooling and removal of solvent. The residue was dissolved in ethyl acetate and washed rapidly with 1.3N HCl (40 ml). The acidic layer was then extracted with ethyl acetate (3×20 ml) and the combined organic layers washed with brine before drying over magnesium sulfate, filtering and removal of solvent in vacuo. The desired product (5.9 g, 94%) was isolated as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07115639B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-e25bdd105f094a92a2614a2391678a3d
Quellennotizuspto-grants-2006_10