HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 2-(1-Methyl-1h-imidazol-5-yl)cyclohexan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(3-Methylimidazol-4-yl)cyclohex-2-en-1-one | HCID 89963299 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(1-Methyl-1h-imidazol-5-yl)cyclohexan-1-ol | HCID 89963398 | 61.1% |
Reaction Steps
To a solution of the 2-(1-methyl-1H-imidazol-5-yl)cyclohex-2-en-1-one (80 mg, 0.454 mmol) prepared in Example 49a in methanol (2.0 mL), sodium borohydride (50 mg, 1.32 mmol) was added at room temperature, and the reaction solution was stirred at room temperature for 30 minutes. To the reaction solution, a saturated aqueous solution of ammonium chloride (20 mL) was added, followed by extraction with dichloromethane (50 mL). The thus obtained organic layer was dried over anhydrous sodium sulfate and vacuum concentrated to yield the title compound (50 mg, 61%) in the form of a trans/cis (2:1) mixture as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889741B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-cb02b9af030046f4bfa6394f54e31ca1 |
| Source note | uspto-grants-2014_11 |