HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1,3-Dibenzylpyrrolidine-3-carboxylic acid amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 1,3-Dibenzylpyrrolidine-3-carboxylic acid | HCID 21979351 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Dibenzylpyrrolidine-3-carboxylic acid amide | HCID 21979009 | 103.9% |
Reaction Steps
A mixture of 1,3-dibenzylpyrrolidine-3-carboxylic acid (Example A28, 4.0 g, 13.5 mmol), 1,1′-carbonyldiimidazole (2.42 g, 14.9 mmol), and triethylamine (2.08 mL, 14.9 mmol) in tetrahydrofuran (100 mL) is heated at reflux for 1.5 hours. The solution is cooled, poured into NH4OH (300 mL), and stirred for 18 hours. The mixture is extracted with chloroform, the organic layer is washed with water, dried, and concentrated to afford 4.13 g of the title compound as an oil; MS El+: m/z 295 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07094780B1 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-02ad2852ead94e6593b17d452a0bcb4b |
| Source note | uspto-grants-2006_08 |