HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859878Generated: November 1, 2026
Sodium Bicarbonate → cis-1-Benzyl-4-methyl-3-aminomethylpyrrolidine
https://huagongshe.com/reaction/859878
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 cooled on an ice bath, a diethyl ether solution (25 mL) of cis-1-benzyl-4-methyl-3-pyrrolidinecarbonitrile (4.11 g) was added dropwise and the mixture was stirred at room temperature for 1 hour. While the reaction mixture was cooled on an ice bath, a saturated aqueous solution of sodium hydrogen carbonate (8 mL) was carefully added dropwise. Following dilution with diethyl ether (100 mL), insoluble materials were collected by filtration and were washed with diethyl ether. The filtrate and the washing solution were combined and the combined solution was concentrated under reduced pressure. The resulting residue was purified on a silica gel column (hexane:ethyl acetate=1:1 shifted to ethyl acetate: methanol=10:1) to give 2.35 g of cis-1-benzyl-4-methyl-3-aminomethylpyrrolidine as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07153851B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-8c7029ad0aef426497edcde90232950d |
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| Source note | uspto-grants-2006_12 |
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