HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 6,6-Dimethyl-4,5,6,7-tetrahydro-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 2-[1-hydroxy-meth-(Z)-ylidene]-5,5-dimethyl-cyclohexanone | HCID 89421039 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6,6-Dimethyl-4,5,6,7-tetrahydro-1H-indazole | HCID 58550437 | 96.1% |
Reaction Steps
To a solution of 2-[1-hydroxy-meth-(Z)-ylidene]-5,5-dimethyl-cyclohexanone (1.64 g, 10.6 mmol) in MeOH (10 mL) was added hydrazine (0.33 mL, 10.6 mmol) dropwise. The exothermic reaction was controlled by intermitant use of an ice bath. The yellow reaction mixture was stirred at room temperature for 30 min then concentrated. The residue was dissolved in CH2Cl2 and washed with water. The organic layer was dried over MgSO4 and concentrated to afford 1.53 g (96%) of 6,6-dimethyl-4,5,6,7-tetrahydro-1H-indazole as a yellow solid. 1H NMR (CDCl3, 300 MHz): δ (ppm) 7.32 (s, 1H), 2.55 (t, J=6.4 Hz, 2H), 2.44 (s, 2H), 1.53 (t, J=6.4 Hz, 2H), 1.01 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658646B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-5ac2f217b8a04778a71cffec92c50d1a |
| Source note | uspto-grants-2014_02 |