Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Benzylpyrrolidin-3-yl 4-methylbenzenesulfonate | HCID 15623668 | — |
| Product | 3-Anilino-1-benzylpyrrolidine | HCID 11184326 | 47.8% |
Reaction Steps
1-Benzyl-3-(p-toluenesulfonyloxy)pyrrolidine (3.3 g) and aniline (1.3 g) were mixed and stirred under heating at 160° C. for 3 hours. After the completion of the reaction, the mixture was cooled to room temperature, and an aqueous potassium carbonate solution was added thereto. The obtained mixture was extracted with chloroform, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was subjected to silica gel column chromatography (chloroform:methanol=40:1). The obtained eluate was concentrated to give 3-anilino-1-benzylpyrrolidine (1.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06468998B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-26282bd65f6e48e1abfb7d157cebbfa4 |
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| Source note | uspto-grants-2002_10 |
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