HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → Indenolol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Isopropylamino-2-hydroxy-1-chloropropane | HCID 12624612 | — |
| Reactant | 1H-Inden-4-ol | HCID 14940863 | — |
| Product | Indenolol | HCID 71955 | — |
Reaction Steps
To a solution of 0.44 g. of 4-hydroxyindene in 4 ml. of an aqueous 10% potassium hydroxide solution there was added 0.65 g. of 1-chloro-2-hydroxy-3-isopropylaminopropane. After stirring the resulting mixture at room temperature for 15 hours, the reaction mixture was extracted with ether, the ether extract was dried with anhydrous sodium carbonate and the ether was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography using acetone as eluent, and 0.23 g. of white crystals of 4-(3-isopropylamino-2-hydroxypropoxy)indene was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04045482 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-bb6cc88547d34f6e87bc95c7f9b44ee6 |
| Source note | uspto-grants-1977_08 |