HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(2-Bromoethyl)indole | HCID 76924 | — |
| Reactant | HCID 13180309 | HCID 13180309 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Indole | HCID 798 | — |
Reaction Steps
A solution of 9.6 g of 3-(2-bromoethyl)indole, 11.5 g of 4-(3,4-dimethylbenzoyl)piperidine hydrochloride and 10.1 g of triethylamine in 300 ml of dimethylformamide is treated according to the manipulative procedure described in Example 3(b) to give an indole, which is purified on a silica gel column, eluted with a 5% methanol-benzene mixture and recrystallized from an ethanol-water mixture to give the solid, mp 172°-173° C., 3-{2-[4-(3,4-dimethylbenzoyl)piperidyl]ethyl}indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04046900 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-9a518436b83845c3a1b16581b09e22f7 |
| Source note | uspto-grants-1977_09 |