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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468566Generated: October 25, 2026

Hydrochloric Acid → N-Boc-3-mesyloxypiperidine

https://huagongshe.com/reaction/468566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-Boc-3-hydroxypiperidineHCID 545699—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventHeptaneHCID 8900—
ProductN-Boc-3-mesyloxypiperidineHCID 56812283.4%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of 216 g of N-BOC-3(R,S)-hydroxypiperidine in 5 l of CH2Cl2 222 ml of triethylamine are added at 0-5° C. 137 g of methanesulfonyl chloride in 300 ml of CH2Cl2 are added dropwise over a period of 45 min, maintaining the temperature at 0-5° C. After additional stirring for 70 minutes 2 l of deionised water are added and the pH is adjusted to 5.9 by addition of about 90 ml of 2 n HCl. The aqueous phase is separated and the organic phase is washed with water. The solution is evaporated to dryness and 270-280 g of an oily residue are obtained. After treating with 1 l of n-heptane crystallization occurs. Crystals are isolated and dried in vacuo. 250 g of N-BOC-3(R,S)-methylsulfonyloxy-piperidine are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08624033B2
Source datasetuspto-grants-2014_01
ORD IDord-6c131f9de07f440991663ec1e7900139
Source noteuspto-grants-2014_01