HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1-Piperidin-4-yl-2,3-dihydro-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 53677180 | HCID 53677180 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-Piperidin-4-yl-2,3-dihydro-1H-indole | HCID 22028603 | 91.4% |
Reaction Steps
A mixture of intermediate 6 (95 g) and potassium hydroxide (194 g) in 2-propanol (1300 ml) was stirred and refluxed for 24 hours. The solvent was evaporated and the residue was dissolved in H2O/CH2Cl2. The organic layer was separated, dried over MgSO4, filtered and evaporated, yielding 64 g (90.4%) of 2,3-dihydro-1-(4-piperidinyl)-1H-indole. A sample (4.5 g) was crystallized from CH3OH and converted into the hydrochloric acid salt (1:1) in 2-propanol and filtered off, yielding 3.0 g of 2,3-dihydro-1-(4-piperidinyl)-1H-indole monohydrochloride (intermediate 7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919788 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-433927c8f7c644dc8ea16810f99615f2 |
| Source note | uspto-grants-1999_07 |