HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → (1R,2S,5R)-5-Methyl-2-(propan-2-yl)cyclohexane-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | (1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyl chloride | HCID 3084750 | — |
| Product | (1R,2S,5R)-5-Methyl-2-(propan-2-yl)cyclohexane-1-carboxamide | HCID 59253413 | — |
Reaction Steps
A 250 mL flask was purged with nitrogen, left under a nitrogen atmosphere, and charged with 13.0 g (0.0641 mol) of (1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyl chloride. While stirring 130 mL of 29% ammonium hydroxide solution was added to the flask. A white precipitate quickly formed, and after stirring overnight the fine white slurry was suction filtered. The filter cake was washed with water (3×50 mL) then dried in a vacuum oven (RT, 5 mm Hg, 3 days) to provide (1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxamide as a white solid with the following spectroscopic properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754259B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-500ac5beb60b499683e61902d6428adc |
| Source note | uspto-grants-2014_06 |