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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1583539Erstellt: 25. Oktober 2026

Hydrochloric Acid → 3-Mercapto-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine

https://huagongshe.com/reaction/1583539

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium MethoxideHCID 10942334—
Edukt3-Acetylthio-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidineHCID 54037145—
LösungsmittelMethanolHCID 887—
Produkt3-Mercapto-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidineHCID 5340089275,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of 30 g of 3-acetylthio-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine in 1000 ml of methanol was cooled to -10° C. A solution of sodium methoxide in methanol (prepared from 1.8 g of sodium) was then added dropwise to the cooled solution, after which the mixture was stirred for 30 minutes, whilst gradually raising the temperature to 0° C. At the end of this time, 65.2 ml of 10% w/v hydrochloric acid were added to the reaction mixture, which was then concentrated to half of its original volume by evaporation in vacuo. A saturated aqueous solution of sodium chloride was added to the concentrate and the mixture was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride and then dried, after which the solvent was distilled off under reduced pressure. The residue was purified by chromatography through a column of silica gel, eluted with a 2:1 by volume mixture of benzene and ethyl acetate, to give 20 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04552873
Quelldatensatzuspto-grants-1985_11
ORD IDord-b688f42ee3874320bf9c622be60a049a
Quellennotizuspto-grants-1985_11