HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20277905, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Methylallylamine | HCID 76141 | — |
| Reactant | n-benzyl-3-bromopropanamide | HCID 236377 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20277905 | HCID 20277905 | 17% |
Reaction Steps
N-Benzyl-3-bromopropanamide (6 g), methallylamine (1.9 g) and triethylamine (3.5 ml) in dimethylformamide (12 ml) were heated together under reflux for 21/4 hr, then poured into ethyl actate (100 ml). The organic phase was washed with water (2×100 ml), saturated brine (100 ml) and dried over magnesium sulphate. Removal of the solvent under reduced pressure gave a yellow oil which produced the title compound in 17% yield after column chromatography using ethyl acetate:ethanol (1:1) as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04524073 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-1c1a9182564646e6a73a3d47b8f5d6fd |
| Source note | uspto-grants-1985_06 |