Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 862Erstellt: 24. Oktober 2026

(Pyrrolidin-3-yl)methanol → benzyl N-[3-(hydroxymethyl)pyrrolidine-1-carboximidoyl]carbamate

https://huagongshe.com/de/reaction/862

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(Pyrrolidin-3-yl)methanolHCID 13400657—
Eduktbenzyl N-(C-methoxycarbonimidoyl)carbamateHCID 139267837—
LösungsmittelTolueneHCID 1140—
Produktbenzyl N-[3-(hydroxymethyl)pyrrolidine-1-carboximidoyl]carbamateHCID 14037908525,2%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

1.01 g (0.01 mole) (3RS)-3-hydroxymethyl pyrrolidine and 2.29 g (0.011 mole) N-benzyloxycarbonyl-O-methylisourea was dissolved (the amine not very soluble) in toluene and heated to 60° C. for three hours followed by stirring at room temperature over night. The mixture was evaporated and the 1H-NMR showed that the reaction was not completed. The mixture was therefore dissolved in 15 ml acetonitrile and heated to 60° C. for three hours followed by stirring at room temperature over night. The solvent was evaporated and the mixture was dissolved in CH2Cl2, washed once with water, dried (Na2 SO4), filtered and evaporated. The crude product was purified by flash chromatography using CH2Cl2 /MeOH 95/5 as eluent to yield 0.70 g (25%) of the product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723444
Quelldatensatzuspto-grants-1998_03
ORD IDord-66270614c8d046a8af9a342eb13c4b24
Quellennotizuspto-grants-1998_03