HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-(4-Benzamidopiperidinoacetyl)-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-4-Piperidylbenzamide | HCID 118120 | — |
| Reactant | 1,1,3,4,4,6-Hexamethyl-7-bromacetyl-1,2,3,4-tetrahydronaphthalene | HCID 21430625 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-(4-Benzamidopiperidinoacetyl)-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene | HCID 21430621 | 24.1% |
Reaction Steps
A mixture of 1,1,3,4,4,6-hexamethyl-7-bromacetyl-1,2,3,4-tetrahydronaphthalene (7 g.), 4-benzamidopiperidine (4.27 g.) and triethylamine (3.5 g.) was refluxed in100 ml. EtOH for 2 hours. The resulting yellow solution was cooled, whereupon the product crystallised. This was recrystallised twice from EtOH/water to give the title compound (2.3 g.) as a pale yellow solid, m.p. 153°(dec.). Analysis Calculated for C30H40N2O2 ; C, 78.22%; H, 8.75%; N, 6.08%. Found: C, 78.29%; H, 8.92%; N, 6.14%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03992389 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-1afb6b98244f4aabb8679724746b5ab4 |
| Source note | uspto-grants-1976_11 |