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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383796Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86661362, compound

https://huagongshe.com/reaction/383796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86661363HCID 86661363—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86661362HCID 86661362—

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of tert-utyl cis-3-cyclohexyl-5-(hydroxymethyl)piperidine-1-carboxylate (431.1 mg) in THF (10 ml) was added TEA (405.0 ml) and MsCl (135.2 ml) at 0° C. After stirring at 0° C. for 1 hour, the insoluble material was filtered off through celite and washed with THF. The filtrate was concentrated to give the crude tert-butyl cis-3-cyclohexyl-5-{[(methylsulfonyl)oxy]methyl}piperidine-1-carboxylate as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367690B2
Source datasetuspto-grants-2013_02
ORD IDord-58c33996ca54486ab409517be86376d6
Source noteuspto-grants-2013_02