HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → HCID 14549839, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 4-{4-[(6-Bromohexyl)oxy]butyl}-N,N-diethylbenzamide | HCID 20071417 | — |
| Product | HCID 14549839 | HCID 14549839 | 76.5% |
Reaction Steps
4-[4-[(6-Bromohexyl)oxy]butyl]-N,N-diethybenzamide (6.0 g) and benzylamine (9.36 g) were stirred under nitrogen at 120° for 30 mins. Excess benzylamine was removed by distillation under reduced pressure. The residual solid was dissolved in ethyl acetate (100 ml) and washed with 8% aqueous sodium bicarbonate (100 ml). The ethyl acetate solution was dried and evaporated to give a yellow oil which was purified by FCC eluting System B (95:5:1) to give the title compound as a yellow oil (4.88 g), t.l.c. (System B 95:5:1) Rf 0.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04908386 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-4a4146e0d23042d298e7249cac6b6311 |
| Source note | uspto-grants-1990_03 |