HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-{2-[4-(2-Toluyl)piperidyl]ethyl}indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(2-Bromoethyl)indole | HCID 76924 | — |
| Reactant | 4-(2-Methylphenyl)piperidine hydrochloride | HCID 21936956 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-{2-[4-(2-Toluyl)piperidyl]ethyl}indole | HCID 20311701 | — |
Reaction Steps
To a stirring solution of 4.2 g of 4-(2-toluyl)piperidine hydrochloride and 4.0 g of triethylamine in 150 ml of dimethylformamide is added 3.8 g of 3-(2-bromoethyl)indole. The resulting solution is stirred at ambient temperature for 70 hours and stirring is continued while 500 ml of water are added dropwise. An oil appears which is extracted from the solution with chloroform, the combined chloroform extracts are dried and the excess chloroform is removed, leaving an oil which crystallizes upon standing. The solid product is recrystallized from cyclohexane and then twice from an ethanol-water mixture to give flakes, mp 111°-112° C., 3-{2-[4-(2-toluyl)piperidyl]ethyl}indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101663 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-576db3d10cd6490eade9423e7c8fa8da |
| Source note | uspto-grants-1978_07 |