HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (Decan-4-yl)hydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | tert-Butyl N'-(1-propyl-heptylidene)-hydrazinecarboxylate | HCID 72599202 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (Decan-4-yl)hydrazine | HCID 21266060 | — |
Reaction Steps
39.41 g (145.7 mmol) of tert-butyl N′-(1-propyl-heptylidene)-hydrazinecarboxylate are dissolved in a mixture of 100 ml of THF and 150 ml of methanol and, after 10.65 g (169 mmol) of sodium cyanoborohydride have been added, the mixture is stirred for 1 hour at room temperature. 100 ml of 6N HCl are added dropwise in the course of 30 minutes and, after the addition has ended, the mixture is refluxed for 1 hour. The mixture is neutralized with 6N NaOH solution, then, after the non-aqueous solvents have been removed, extracted three times with dichloromethane, and, after the mixture has been dried over sodium sulphate, the solvent is removed in vacuo. This gives 23.90 g (95%) of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06174884B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-3a87f0a3baa74b9aab68e93d12729bcb |
| Source note | uspto-grants-2001_01 |