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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30103Generated: October 26, 2026

Trifluoroacetic acid → [1-(Methylsulfonyl)piperidin-4-yl]amine trifluoroacetate

https://huagongshe.com/reaction/30103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl [1-(methanesulfonyl)piperidin-4-yl]carbamateHCID 25250149—
SolventDichloromethaneHCID 6344—
Product[1-(Methylsulfonyl)piperidin-4-yl]amine trifluoroacetateHCID 11975076100%

Reaction Steps

A suspension of (1-methanesulfonyl-piperidin-4-yl)-carbamic acid tert-butyl ester (1.14 g, 4.1 mmol, from above) in methylene chloride (15 mL) was treated at room temperature with trifluoroacetic acid (5.3 mL). After stirring for 2 hours, all solvent was removed and the residue was triturated with ether. This was filtered, washed with ether and dried in vacuum to give 1-methanesulfonyl-piperidin-4-ylamine; compound with trifluoro-acetic acid (1.20 g, 100% yield). HRMS, observed: 177.0692; Calcd for M+: 177.0698.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423051B2
Source datasetuspto-grants-2008_09
ORD IDord-74e5a278559740078390b7de6cb938b2
Source noteuspto-grants-2008_09