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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | cis-1-Benzyl-4-methyl-3-pyrrolidinecarbonitrile | HCID 66704969 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | cis-1-Benzyl-4-methyl-3-aminomethylpyrrolidine | HCID 15206166 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514451B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-97c4a5ec9e2444b39fe05d7ac05eda77 |
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| Source note | uspto-grants-2009_04 |
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