HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylbenzylamine → 5-acetonyl-3-(N-benzyl-N-methylamino)methyl-1,2,4-oxadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Acetonyl-3-chloromethyl-1,2,4-oxadiazole | HCID 13824705 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-acetonyl-3-(N-benzyl-N-methylamino)methyl-1,2,4-oxadiazole | HCID 20161256 | 65.6% |
Reaction Steps
A mixture of 800 mg of 5-acetonyl-3-chloromethyl-1,2,4-oxadiazole, 720 mg of N-methylbenzylamine and 1.0 g of triethylamine in 5 ml of DMF was stirred at room temperature for 8 hours. The reaction mixture was then poured into ice-water and the resultant mixture was extracted with ethyl acetate. The extracts were washed with water, dried over magnesium sulfate and concentrated in vacuo to yield a brown oil. Chromatography on silica gel using chloroform-methanol (20:1, v/v) as eluent afforded 780 mg of 5-acetonyl-3-(N-benzyl-N-methylamino)methyl-1,2,4-oxadiazole as a colorless oil, IR νmaxneat cm-1 : 1730, 1635, 1580, 1545, 1450, 1360.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04705786 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-303c850ae3a546e8b488f5e8da837353 |
| Source note | uspto-grants-1987_11 |