HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 5-[4-(4-Benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 5-Bromoindole | HCID 24905 | — |
| Reactant | 1-(Benzenesulfonyl)-5-bromo-1H-indole | HCID 2776210 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 5-[4-(4-Benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole | HCID 10641073 | — |
Reaction Steps
1-Benzenesulfonyl-5-bromoindole. A mixture of 5-bromoindole (5 g, 25.5 mmol) and tetra-n-butylammonium hydrogen sulfate (866 mg, 2.55 mmol) in 50% NaOH (50 mL) and toluene (200 mL) is stirred at room temperature for 5 min. Benzenesulfonyl chloride (3.57 mL, 28 mmol) is added and the mixture stirred for 1 hr. The mixture is diluted with water (500 mL) and extracted with EtOAc (3×100 mL). The extracts are washed with brine (250 mL), dried over MgSO4, filtered and evaporated to a yellow oil. The oil is purified by medium-pressure column chromatography on silica gel eluting with 10% EtOAc/hexanes to give the title compound as a white solid (7.81 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06130234 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-fd3c74e9053c4d6b856d6c9a3df5f433 |
| Source note | uspto-grants-2000_10 |