HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 6-[4-(4-(5-Bromoindol-3-yl)butyl)piperazino]-1,4-benzodioxane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-[4-(4-(1-Benzenesulfonyl-5-bromoindol-3-yl)butyl)piperazino]-1,4-benzodioxane | HCID 19797346 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-[4-(4-(5-Bromoindol-3-yl)butyl)piperazino]-1,4-benzodioxane | HCID 19797312 | — |
Reaction Steps
4.7 g of 6-[4-(4-(1-benzenesulfonyl-5-bromoindol-3-yl)butyl)piperazino]-1,4-benzodioxane is boiled for 16 hours with 1.5 g of KOH in aqueous ethanol solution, worked up in the conventional manner and gives 6-[4-(4-(5-bromoindol-3-yl)butyl)piperazino]-1,4-benzodioxane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05242925 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-e8ab03e55e3649428504c580d6dadc51 |
| Source note | uspto-grants-1993_09 |