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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73524Generated: October 30, 2026

Benzyl chloroformate → HCID 58386793, compound

https://huagongshe.com/reaction/73524

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 numberUS08829193B2
Source datasetuspto-grants-2014_09
ORD IDord-15baeb56258e4d66a9364f5a7ca11f14
Source noteuspto-grants-2014_09