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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980745Generated: October 26, 2026

Carbon Dioxide → N,N-diethyl-1-(phenylmethyl)-3-pyrrolidinemethanamine

https://huagongshe.com/reaction/980745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant4-MethylmorpholineHCID 7972—
ReactantDiethylamineHCID 8021—
ReactantEthyl chloroformateHCID 10928—
Reactant1-Benzyl-5-oxo-pyrrolidine-3-carboxylic acidHCID 99024—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN,N-diethyl-1-(phenylmethyl)-3-pyrrolidinemethanamineHCID 1407547269.8%

Reaction Conditions

Temperature-25 °C

Reaction Steps

To a solution of 32.9 g (0.15 mole) 5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxylic acid [J. Org. Chem., 26, 1519 (1961)] and 300 ml of dichloromethane was added 15.2 g (0.15 mole) of N-methylmorpholine. After 15 minutes the solution was cooled to -25° C. and 16.3 g (0.15 mole) of ethyl chloroformate was added. After an additional ten minutes, a solution of 13.5 g (0.18 mole) of diethylamine and 18 ml dichloromethane was added to the reaction. Carbon dioxide was evolved and after 1.5 h another 10 g (0.13 mole) of diethylamine in 10 ml of dichloromethane was added. The reaction was stirred four hours, washed with 1N sodium hydroxide, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was added to a suspension of 17.4 g (0.46 mole) of lithium aluminum hydride and 210 ml anhydrous tetrahydrofuran. The reaction was refluxed overnight then cooled to room temperature. The cooled solution was quenched with 17.4 ml water, 17.4 ml 15% sodium hydroxide, and 52.2 ml water. The resulting precipitate was filtered and washed with ethyl alcohol. The filtrate was concentrated under reduced pressure, taken up in dichloromethane, dried over magnesium sulfate. The solvent was removed under vacuum giving 25.8 g (69%) of N,N-diethyl-1-(phenylmethyl)-3-pyrrolidinemethanamine as a yellow oil. This material was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04638067
Source datasetuspto-grants-1987_01
ORD IDord-9b25b21de4984043881c81c4fb637e0a
Source noteuspto-grants-1987_01