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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560189Generated: October 25, 2026

Sodium Bicarbonate → C-Phenyl-C-(3-pyrrolidin-1-yl-oxetan-3-yl)-methylamine

https://huagongshe.com/reaction/560189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Cyano-3-(pyrrolidin-1-YL)oxetaneHCID 59197919—
ReactantHCID 178506676HCID 178506676—
SolventTetrahydrofuranHCID 8028—
ProductC-Phenyl-C-(3-pyrrolidin-1-yl-oxetan-3-yl)-methylamineHCID 59197932—

Reaction Steps

3-Pyrrolidin-1-yl-oxetane-3-carbonitrile (intermediate A, 1.6 g, 91% purity, 10 mmol) was dissolved in 10 mL tetrahydrofurane. Phenyllithium (2M in dibutylether, 9.8 mL, 20 mmol) was added dropwise at −5° C. The reaction mixture was stirred at room temperature for 1.5 hours and poured into cold saturated sodium bicarbonate solution. The mixture was extracted three times with ethyl acetate. The combined organic phases were dried on sodium sulfate, filtered and evaporated. The residue was dissolved in 35 mL methanol and sodiumborohydride (0.77 g, 20 mmol) was added portion-wise at 0° C. The reaction mixture was stirred at room temperature for 2 hours and quenched by addition of water. The solvent was evaporated off. The residue was taken up in water and ethyl acetate and was extracted three times with ethyl acetate. The combined organic phases were dried on sodium sulfate, filtered and evaporated. The crude product (brown oil, 2.26 g, 99%) was used for the next step without further purification, MS: m/e=216.3 [(M−NH2)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063098B2
Source datasetuspto-grants-2011_11
ORD IDord-e2152e1c1c12418e91a40e92a7bbc5bd
Source noteuspto-grants-2011_11