HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1-(3-Bromophenyl)cyclohexanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 43345643 | HCID 43345643 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 1-(3-Bromophenyl)cyclohexanecarboxamide | HCID 58909432 | — |
Reaction Steps
With overhead stirrer, a mixture of crude product from step 1, above, (380 g, 1207 mmol), powdered KOH (720 g) and t-BuOH (2.5 L) was heated at reflux overnight. See Hall, J. H.; Gisler, M. A simple method for converting nitriles to amides. Hydrolysis with potassium hydroxide in tert-butyl alcohol. J. Org. Chem. 1976, 41, 3769-3770. If deemed complete by GC analysis, it was cooled with ice-water (cool slowly to avoid shock to the glass), quenched with ice-water (1500 mL). The quenched mixture was then extracted with MTBE (3.5 L+1.5 L). MTBE layers were concentrated to a yellow solid, 390 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07544717B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-3cedd4ad77404918b787e475270c4ca1 |
| Source note | uspto-grants-2009_06 |