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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108772Generated: October 30, 2026

Sodium Bicarbonate → cis-1-Benzyl-4-methyl-3-aminomethylpyrrolidine

https://huagongshe.com/reaction/2108772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantAluminium lithium hydrideHCID 21226445—
Reactantcis-1-Benzyl-4-methyl-3-pyrrolidinecarbonitrileHCID 66704969—
SolventDiethyl EtherHCID 3283—
Productcis-1-Benzyl-4-methyl-3-aminomethylpyrrolidineHCID 1520616656%

Reaction Steps

Lithium aluminum hydride (80%, 3.89 g) was suspended in diethyl ether (90 mL). While the suspension was chilled in an ice bath, cis-1-benzyl-4-methyl-3-pyrrolidinecarbonitrile (4.11 g) in diethyl ether (25 mL) was added dropwise and the mixture was stirred at room temperature for 1 hour. Subsequently, a saturated aqueous solution of sodium bicarbonate (8 mL) was carefully added dropwise while the reaction mixture was chilled in an ice water bath. The reaction mixture was then diluted with diethyl ether (100 mL) and the insoluble material was filtered and was washed with diethyl ether. The filtrate and the washings were combined and the organic layer was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane: ethyl acetate=1:1->ethyl acetate: methanol=10:1) to give cis-1-benzyl-4-methyl-3-aminomethylpyrrolidine as a pale yellow oil (2.35 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514451B2
Source datasetuspto-grants-2009_04
ORD IDord-97c4a5ec9e2444b39fe05d7ac05eda77
Source noteuspto-grants-2009_04