HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-[4-(4-Benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Benzenesulfonyl-5-[4-(4-benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole | HCID 18427956 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-[4-(4-Benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole | HCID 10641073 | 80.4% |
Reaction Steps
A mixture of 1-benzenesulfonyl-5-[4-(4-benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole (1.49 g, 3.1 mmol) is stirred in EtOH (200 mL) and 50% NaOH (1 mL) at room temperature for 3 days. Most of the EtOH is evaporated and the residue diluted with water (200 mL). The precipitate is filtered off and washed copiously with water. The precipitate is recrystallized from hot EtOH to give the title compound as an off-white solid (854 mg): mp 165-166° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06448270B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-108c3faaac79487d9efe13dbf5711002 |
| Source note | uspto-grants-2002_09 |