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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920162Generated: October 30, 2026

Benzyl chloroformate → HCID 58386793, compound

https://huagongshe.com/reaction/1920162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
Reactant(3R,5R)-5-((tert-Butyldimethylsilyl)oxy)piperidin-3-olHCID 21103800—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58386793HCID 5838679374%

Reaction Steps

To a solution of (3R,5R)-5-(tert-butyldimethylsilyloxy)piperidin-3-ol (1 eq) in 20 mL of 1,4-dioxane and 8 mL of water was added benzyl chloroformate (1.5 eq). The mixture was stirred at room temperature for 4 hours. The crude mixture was diluted with 100 mL of EtOAc, washed with brine, then dried over anhydrous MgSO4, filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (EtOAc:hexanes=1:3) to yield (3R,5R)-benzyl 3-(tert-butyldimethylsilyloxy)-5-hydroxypiperidine-1-carboxylate (74%). LC/MS (m/z): 366.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168794B2
Source datasetuspto-grants-2012_05
ORD IDord-9a5ff56b4b1b40b296ede70805793dbc
Source noteuspto-grants-2012_05