HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 3-(3-Amino-3-methylbutoxy)-6-chloropyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | 3-Amino-3-methylbutan-1-ol | HCID 641000 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 3-(3-Amino-3-methylbutoxy)-6-chloropyridazine | HCID 10036235 | 84.8% |
Reaction Steps
A mixture of 0.62 g of 60% sodium hydride, 1.91 g of 3,6-dichloropyridazine and 10 ml of benzene was stirred while being cooled with ice, and a solution consisting of 1.32 g of 3-amino-3-methylbutanol, 3 ml of t-butanol and 5 ml of benzene was added dropwise. After stirring at room temperature for 30 minutes, ether was added to the reaction mixture, and the solid was removed by filtration with Hyflo Super-Cel. The filtrate was concentrated under reduced pressure. n-Hexane was added to the resulting oily product, and the mixture was allowed to stand to give 2.34 g of 3-(3-amino-3-methylbutoxy)-6-chloropyridazine as colorless crystals having a melting point of 63.5° to 65.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04599333 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-8e608fddabfc492fb74b8e5d183f2822 |
| Source note | uspto-grants-1986_07 |