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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038074Generated: October 30, 2026

Trifluoroacetic acid → 1-Benzyl-3-dimethylaminomethyl-pyrrolidine-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/1038074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Dimethylaminomethyl-acrylic acid methyl esterHCID 20669687—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-3-dimethylaminomethyl-pyrrolidine-3-carboxylic acid methyl esterHCID 5768618478%

Reaction Steps

To a cold solution of 2-dimethylaminomethyl-acrylic acid methyl ester (0.266 g, 1.86 mmol) and N-(methoxymethyl)-N-(trimethylsilylmethyl)benzyl-amine (1.43 ml, 5.59 mmol) in dichloromethane (25 ml) was added at 0° C. trifluoroacetic acid (83 μl, 1.12 mmol). The resulting solution was warmed to room temperature and stirred for 72 hours. Saturated aq. NaHCO3 (60 ml) was added to the reaction mixture and stirred for 10 minutes. Diluted with dichloromethane (50 ml) and the organic layer was separated. The organic layer was dried over Na2SO4, filtered and concentrated. The crude product was purified by column chromatography on silica get eluting with a solution of ethyl acetate in hexanes (1:2) followed by CH2Cl2/MeOH/NH4OH (9/1/0.01) to give the title compound (400 mg, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546404B2
Source datasetuspto-grants-2013_10
ORD IDord-88c25da0e3c54578a03b0f68e8958b8b
Source noteuspto-grants-2013_10