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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344290Generated: October 30, 2026

Water → cis-l-Tert-butoxycarbonyl-3-hydroxy-4-methanesulfonyloxymethylpiperidine

https://huagongshe.com/reaction/344290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,1-Dimethylethyl 3-hydroxy-4-(hydroxymethyl)-1-piperidinecarboxylateHCID 15481060—
SolventDichloromethaneHCID 6344—
Productcis-l-Tert-butoxycarbonyl-3-hydroxy-4-methanesulfonyloxymethylpiperidineHCID 86753635—
Producttrans-1-Tert-butoxycarbonyl-3-hydroxy-4-methanesulfonyloxymethylpiperidineHCID 86753636—

Reaction Steps

To a solution of 1-tert-butoxycarbonyl-3-hydroxy-4-hydroxymethylpiperidine (6.5 g) and triethylamine (5.87 ml) in dichloromethane (100 ml) was added dropwise methanesulfonyl chloride (3.54 g) under ice-cooling, and the resulting mixture was stirred at room temperature for 6 hr. Water was added to the reaction mixture and the mixture was extracted with chloroform. The organic layer was washed with brine and dried. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (chloroform:methanol=40:1) to give 4.44 g of cis-l-tert-butoxycarbonyl-3-hydroxy-4-methanesulfonyloxymethylpiperidine and 0.93 g of trans-1-tert-butoxycarbonyl-3-hydroxy-4-methanesulfonyloxymethylpiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05864039
Source datasetuspto-grants-1999_01
ORD IDord-cb436ae2cbc1490ba74c7a83af05b90a
Source noteuspto-grants-1999_01