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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322486Generated: October 29, 2026

Trimethylamine → 1-(Naphthalene-1-sulfonyl)-pyrrolidin-3-ylamine

https://huagongshe.com/reaction/322486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylamineHCID 1146—
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-Naphthalenesulfonyl chlorideHCID 66560—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl pyrrolidine-3-carboxylateHCID 22394392—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventChloroform methanolHCID 21584188—
Product1-(Naphthalene-1-sulfonyl)-pyrrolidin-3-ylamineHCID 5724180223%

Reaction Steps

To a solution of 1-naphthalenesulfonyl chloride (1.0 g, 5.4 mmol) in 50 ml of CH2Cl2 with 2 ml of trimethylamine was added 3-t-butoxycarbonylpyrrolidine (1.5 g, 6.5 mmol) in a portion and the resulting solution was stirred at reflux for 48 h. Reaction mixture was concentrated in vacuo, yielding oily mixture which was partioned between 100 ml of EtOAc and NaHCO3 sat'd aqueous solution. Organic layer was separated, dried over Na2SO4 and concentrated in vacuo to provide an oil, which was redissolved in 20 ml of CH2Cl2. Toward this solution was added 1 ml of trifluoroacetic acid and the resulting solution was stirred for 2 h at 25° C. Reaction mixture was concentrated in vacuo, providing a brown oil, which was dissolved in EtOAc and washed with aqueous NaOH. organic layer was concentrated in vacuo to yield an oil which was subjected to column chromatography (30% MeOH/CHCl3) to provide 0.17 g (23%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211241B1
Source datasetuspto-grants-2001_04
ORD IDord-babfea74bc6a43e3af053c0b6d2b5277
Source noteuspto-grants-2001_04