HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 12891848, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Chloro-N,N-dimethylethylamine | HCID 7901 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 23470342 | HCID 23470342 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 12891848 | HCID 12891848 | — |
Reaction Steps
The 3-benzoyloxy-9-[2-(dimethylamino)ethyl]-1,2,3,4-tetrahydrocarbazole was prepared by following an alkylation procedure similar to that described in Example 11 and using 13.1 g. of 3-benzoyloxy-1,2,3,4-tetrahydrocarbazole and 1.93 g. of sodium hydride (50% in mineral oil) in 150 ml. of dimethylformamide, and 4.9 g. of (dimethylamino)ethyl chloride in 10 ml. of benzene. An ethereal solution of the crude product was filtered through alumina and the concentrated ethereal eluate was treated with ethereal hydrogen chloride to give after recrystallizaton from isopropyl alcohol - ether 5.6 g. of 3-benzoyloxy-9-[2-(dimethylaino)ethyl]-1,2,3,4-tetrahydrocarbazole hydrochloride, m.p. 222°-225°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03959309 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-8e7680b152374e8a83cee160f89ff4d2 |
| Source note | uspto-grants-1976_05 |