HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromopropane → (2-Methylpent-2-yl)hydrazine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Acetazine | HCID 79085 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178455851 | HCID 178455851 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2-Methylpent-2-yl)hydrazine hydrochloride | HCID 19908394 | — |
Reaction Steps
Acetone azine (93 g) is added dropwise under reflux to a solution of propylmagnesium bromide, prepared from 44.3 g of magnesium and 224 g of propyl bromide in 350 ml of ether. After heating under reflux for 3 days, the mixture is poured into an ice-cooled aqueous ammonium chloride solution (500 ml) and the product is extracted using ether. The ether phase is concentrated, and the oily residue is stirred at room temperature for 2 h in 200 ml of water and 100 ml of conc. hydrochloric acid. The non-basic components are removed using tert-butyl methyl ether and the aqueous solution is concentrated on a rotary evaporator.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05091398 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-560a288de979411ab1029e56f1c28a9d |
| Source note | uspto-grants-1992_02 |