HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-Acetamido-7-pyrrolidin-1-yl-5,6,7,8-tetrahydronaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 8-Acetamido-2-tetralone | HCID 13424111 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Benzene dimethylformamide | HCID 19608675 | — |
| Product | 1-Acetamido-7-pyrrolidin-1-yl-5,6,7,8-tetrahydronaphthalene | HCID 19696246 | 69.7% |
Reaction Steps
A mixture of 8-acetamido-2-tetralone (0.4 g, 2 mmol), pyrrolidine (0.28 g, 4 mmol) and tosic acid (10 mg) in benzene:DMF (5:1, 12 mL) was heated at reflux with a Dean-Stark trap for 4 h. The solvent was evaporated and the residue dissolved in 1:1 MeOH:THF (10 mL). Acetic acid (1 mL) and sodium cyanoborohydride (0.25 g, 4 mmol) were added, and the reaction stirred for 16 h. The solvent was evaporated and the residue taken up in water:methylene chloride. The aqueous layer was basified with 12.5% NaOH, and back extracted. The combined organic phase was dried over sodium sulfate, filtered and evaporated. The residue solidified upon standing, and was crystallized from tolune:hexane to give the product (0.36 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05721234 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-fa30521bf41b4b8b86dac3d46a1e75a9 |
| Source note | uspto-grants-1998_02 |