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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Cyano-3-(pyrrolidin-1-YL)oxetane | HCID 59197919 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | C-Phenyl-C-(3-pyrrolidin-1-yl-oxetan-3-yl)-methylamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063098B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-e2152e1c1c12418e91a40e92a7bbc5bd |
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| Source note | uspto-grants-2011_11 |
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