Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431753Generated: October 25, 2026

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

https://huagongshe.com/reaction/431753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(2R,4R)-1-((benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acidHCID 688416—
SolventDimethylformamideHCID 6228—
SolventEthyl acetate hexaneHCID 21226206—
Productcis4-(tert-butyldimethylsilyloxy)-N-benzyloxycarbonyl-D-prolineHCID 6999564189.5%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660759B1
Source datasetuspto-grants-2003_12
ORD IDord-ce1db149d5d3404ab6fb24f15fa37f3a
Source noteuspto-grants-2003_12