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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 431753Erstellt: 26. Oktober 2026

Imidazole → cis4-(tert-butyldimethylsilyloxy)-N-benzyloxycarbonyl-D-proline

https://huagongshe.com/reaction/431753

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
Edukt(2R,4R)-1-((benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acidHCID 688416—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produktcis4-(tert-butyldimethylsilyloxy)-N-benzyloxycarbonyl-D-prolineHCID 6999564189,5%

Reaktionsschritte

To a mixture of cis4-hydroxy-N-benzyloxycarbonyl-D-proline (18.74 g) and imidazole (11.56 g) in DMF (100 mL) was added TBDMSCl (23.36 g) at 5° C. After stirring at room temperature for 16 hours, the reaction mixture was diluted with EtOAc-hexane (1:1, 600 mL), washed with 1N HCl, water and brine, dried (MgSO4), and evaporated in vacuo. The residue was dissolved in MeOH-THF (3:1, 400 mL). To the solution was added an aqueous solution (100 mL) of K2CO3 (9.77 g) at 5° C., and the mixture was stirred at the same temperature for 1 hour. The organic solvent was evaporated, and the residue was adjusted to pH 2 by the addition of 3N HCl, and extracted with EtOAc. The organic layer was washed with water and brine, dried (MgSO4), and evaporated in vacuo. The residue was purified by silica gal column chromatography to give cis-4-(tert-butyldimethylsilyloxy)-N-benzyloxycarbonyl-D-proline (23.99 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06660759B1
Quelldatensatzuspto-grants-2003_12
ORD IDord-ce1db149d5d3404ab6fb24f15fa37f3a
Quellennotizuspto-grants-2003_12