HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (S)-3-(4-bromophenyl)cyclopentanone oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | (S)-3-(4-Bromophenyl)cyclopentan-1-one | HCID 25002103 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | (S)-3-(4-bromophenyl)cyclopentanone oxime | HCID 86671372 | 95.2% |
Reaction Steps
A slurry of (S)-3-(4-bromophenyl)cyclopentanone (prepared according to J. Org. Chem., 2009, 74, 929; 10.9 g, 45.5 mmol), MeOH (110 mL), sodium acetate (5.59 g, 68.2 mmol), and hydroxylamine hydrochloride (4.74 g, 68.2 mmol) was stirred at room temperature. After 10 minutes, LCMS showed complete reaction. Diluted with MTBE (300 mL) and washed with water (100 mL) and brine (50 mL). The organic layer was dried (Na2SO4), filtered, and concentrated. The residue was purified by silica gel chromatography (gradient elution, 25-50% EtOAc/hexanes) to afford the title compound (11.0 g, 43.3 mmol, 95%). MS (DCI) m/z 254 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802711B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-1b061fa03ab84f1db8c8abc4bdbe0663 |
| Source note | uspto-grants-2014_08 |