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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499897Generated: October 30, 2026

Water → 1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine

https://huagongshe.com/reaction/499897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDichloromethaneHCID 6344—
Product1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 418486990%

Reaction Steps

tert-Butyl 4-hydroxypiperidine-1-carboxylate (2.5 g, mmol) and triethylamine (2.1 mL, 15 mmol) were dissolved in dichloromethane (30 mL). To the solution was added a solution of methanesulfonyl chloride (1.2 mL, 15 mmol) in dichloromethane (10 mL), followed by stirring for hours, while the temperature was raised to room temperature. To the reaction mixture was added water (50 mL), and the mixture was stirred for 30 minutes, followed by liquid separation. The organic layer was washed successively with 0.50 mol/L hydrochloric acid (40 mL×2) and a saturated aqueous solution of sodium hydrogencarbonate (10 mL), dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. To the resulting residue was added a mixed solvent of ethyl acetate and hexane (15 mL, ethyl acetate/hexane=1/2), and the precipitated solid was filtered to obtain tert-butyl 4-(methylsulfonyloxy)piperidine-1-carboxylate (3.1 g, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767693B2
Source datasetuspto-grants-2010_08
ORD IDord-bba4cd5d2bdc498f9870f1b2d476f4b7
Source noteuspto-grants-2010_08