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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712555Generated: November 2, 2026

Methylamine → 1-[(3R)-1-Benzylpyrrolidin-3-yl]methanamine

https://huagongshe.com/reaction/1712555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant(S)-1-Benzyl-3-[(P-tolylsulfonyl)oxy]pyrrolidineHCID 10382042—
SolventEthanolHCID 702—
Product1-[(3R)-1-Benzylpyrrolidin-3-yl]methanamineHCID 1519423—

Reaction Conditions

Temperature140 °C

Reaction Steps

An autoclave is initially charged with 6.20 ml of methylamine solution in ethanol and a solution of 2.000 g of (S)-1-benzylpyrrolidin-3-yl toluene-4-sulphonate in 2 ml of ethanol. The reaction solution is subsequently heated to 140° C. over 15 hours. The reaction solution is cooled to room temperature and concentrated to dryness, and the residue is taken up in 10 ml of water. The aqueous solution is extracted with dichloromethane (2×10 ml). The aqueous phase is then admixed with 1 g of potassium carbonate and the suspension is stirred at room temperature over 5 minutes. The solid is filtered off and the filtrate is extracted with dichloromethane (2×10 ml). The combined organic phases are dried over sodium sulphate and concentrated by evaporation. The residue is purified by means of flash chromatography (SiO2 60F). The title compound is obtained as a yellow oil. Rf=0.14 (200:20:1 dichloromethane-methanol-25% conc. ammonia).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790715B2
Source datasetuspto-grants-2010_09
ORD IDord-eb0a8211e3ab4dba96d17da45a502d8e
Source noteuspto-grants-2010_09