HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → 4-(Aminomethyl)-3-cyclopropyl-1,2,4-oxadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | N-[(3-cyclopropyl-1,2,4-oxadiazol-5-yl)methyl]phthalimide | HCID 22713498 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-(Aminomethyl)-3-cyclopropyl-1,2,4-oxadiazole | HCID 22713490 | — |
Reaction Steps
N-[(3-Cyclopropyl-1,2,4-oxadiazol-5-yl)methyl]phthalimide (104 g, 387 mmol) was dissolved in 1,2-dichloroethane (500 mL), N-methylhydrazine (22.4 mL, 426 mmol) was added and the solution was refluxed for 5 h. The suspension was cooled in ice, the precipitate (2-methyl-2,3-dihydro-phthalazine-1,4-dione) was filtered off and washed with 1,2-dichloroethane (100 mL). The filtrate was evaporated and the residue distilled at 70° C./0.4 mbar (bath-T 100-150° C). Yield: 39.3 g (73%). m/z 139 (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06743789B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-690efa1200264a80a13c5dfe52644e48 |
| Source note | uspto-grants-2004_06 |