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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975645Generated: October 30, 2026

Water → (2R,4R)-1-benzyl-2-(2-hydroxyethyl)-4-(t-butyldimethylsilyloxy)pyrrolidine

https://huagongshe.com/reaction/975645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactant(2S,4R)-1-benzyl-2-vinyl-4-(t-butyldimethylsilyloxy)pyrrolidineHCID 11726876—
ReactantSodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
SolventTetrahydrofuranHCID 8028—
Product(2R,4R)-1-benzyl-2-(2-hydroxyethyl)-4-(t-butyldimethylsilyloxy)pyrrolidineHCID 5418095982.3%

Reaction Steps

To a solution of (2S,4R)-1-benzyl-2-vinyl-4-(t-butyldimethylsilyloxy)pyrrolidine (24.03 g) in tetrahydrofuran (120 ml) was added 0.5M solution of 9-borabicyclo[3.3.1]nonane in tetrahydrofuran (318 ml) at 0°~5° C. with stirring and then stirred at ambient temperature for 4 hours. To the reaction mixture were added water (200 ml) and sodium perborate tetrahydrate (87 g) at ambient temperature with stirring vigorously and then the mixture was stirred at the same temperature for 12 hours. The insoluble material was filtered off, and the filtrate was separated. The organic layer was dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue was purified by silica gel chromatography eluting with a mixture of n-hexane and ethyl acetate (1:1, V/V) to give (2R,4R)-1-benzyl-2-(2-hydroxyethyl)-4-(t-butyldimethylsilyloxy)pyrrolidine (20.89 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608056
Source datasetuspto-grants-1997_03
ORD IDord-123aa35c660c413fb775d8ea20ecb96f
Source noteuspto-grants-1997_03