Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | 2-Methylbenzenesulfonic acid hydrate | HCID 12496995 | — |
| Reactant | HCID 53645448 | HCID 53645448 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 289865 | HCID 289865 | — |
Reaction Steps
Place 2-hydroxy-3,3-dimethyl-cyclopentanone (1.044 g, 7.86 mmol), cyclohexylamine (1.91 ml, 16.51 mmol) and toluenesulfonic acid monohydrate (0.152 g, 0.1 mmol) in EtOH (4 mL) in a microwave reactor. Stir for 1 hour at 150° C. Quench with 1N HCl and extract with ethyl acetate. Wash the extract with NaHCO3, brine. Dry over magnesium sulfate, filter, and concentrate to afford N-cyclohexyl-2,4-dihydroxy-3,3-dimethyl-butyramide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07713979B2 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-97a5dda0d18c43b6a17d06eeefbf8222 |
|---|
| Source note | uspto-grants-2010_05 |
|---|