Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815145Generated: October 30, 2026

Methanesulfonyl chloride → Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1815145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylateHCID 2765838—

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolved 1-Boc-4-hydroxymethyl-piperidine in anhydrous CH2Cl2 (50 ml) and TEA (4.5 ml) and cooled to 0° C. Mesyl chloride (840 μl) was added and the mixture was stirred for 15 min then at RT for 45 min. The mixture was washed with brine/1N HCl and then brine, dried over Na2SO4, concentrated in vacuo and dried under high vacuum to provide 1-Boc-4-methylsulfonyloxymethyl-piperidine as a yellow orange thick oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878714B2
Source datasetuspto-grants-2005_04
ORD IDord-e32a54bbe57b49ca9ebeeda4d7537e8f
Source noteuspto-grants-2005_04