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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012285Generated: October 30, 2026

Water → tert-Butyl 3-(tosyloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1012285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant1-Boc-3-hydroxypiperidineHCID 545699—
SolventChloroformHCID 6212—
Producttert-Butyl 3-(tosyloxy)piperidine-1-carboxylateHCID 2046824328.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of tert-butyl 3-hydroxypiperidine-1-carboxylate (2.00 g, 9.94 mmol) in chloroform (20 ml) were successively added p-toluenesulfonyl chloride (2.27 g, 11.9 mmol) and triethylamine (1.66 ml, 11.9 mmol) at 0° C., and the mixture was stirred at 70° C. for 9 hr. The reaction mixture was allowed to cool to room temperature, water was added to the reaction mixture and the mixture was extracted with chloroform. The organic layer was successively washed with water and saturated brine and dried over anhydrous magnesium sulfate. After filtration, the solvent was concentrated under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate:hexane=1:1) to give tert-butyl 3-(toluene-4-sulfonyloxy)piperidine-1-carboxylate (1.00 g, yield 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977331B1
Source datasetuspto-grants-2011_07
ORD IDord-df199b96dc60464aa19642e23f0ecc61
Source noteuspto-grants-2011_07