Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657266Generated: November 1, 2026

Methanesulfonic Acid → N-t-butyl-3,3-diphenylcyclopentylamine methanesulfonate

https://huagongshe.com/reaction/1657266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantN-t-butyl-3,3-diphenylcyclopentylamineHCID 10379659—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductN-t-butyl-3,3-diphenylcyclopentylamine methanesulfonateHCID 1978746489.5%

Reaction Steps

To a suspension of (-)-N-t-butyl-4,4-diphenyl-2-cyclopentenylamine methanesulfonate (0.70 g) in ethyl acetate was added 2N sodium hydroxide aqueous solution (10 ml), and the organic layer was separated. The solution was washed with brine and hydrogenated over 10% palladium-on-carbon (0.06 g) to give (-)-N-t-butyl-3,3-diphenylcyclopentylamine (0.53 g). To a solution of (-)-N-t-butyl-3,3-diphenylcyclopentylamine (0.53 g) in chloroform was added a solution of methanesulfonic acid (174 mg) in methanol. The solvent was evaporated in vacuo and triturated with diethyl ether to give (-)-N-t-butyl-3,3-diphenylcyclopentylamine methanesulfonate (0.63 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256824
Source datasetuspto-grants-1993_10
ORD IDord-1634c3adb6ae45d4b58360617a045582
Source noteuspto-grants-1993_10