HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → 3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Piperonylamine | HCID 2723901 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indole | HCID 2761023 | — |
Reaction Steps
30 g (0.26 mol) of indole were dissolved in a solution of potassium hydroxide (77.6 g, 1.38 mol) in methanol (692 ml). 4-piperidone monohydrate hydrochloride (102.3 g, 0.66 mol) was added in one portion and the mixture was heated to reflux for 5 h. Potassium chloride precipitated upon cooling at room temperature and it was filtered off. The liquid phase was concentrated until only one third of the liquid remained in the round-bottom flask. The solid formed during the concentration of the liquid phase was filtered and washed thoroughly with ethanol and, finally, with ethyl ether. 31.9 g (63% of yield) of the final product were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560471B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-5d424983c19e4484a8c8c5c927e205be |
| Source note | uspto-grants-2009_07 |