HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexyl methyl ketone → 2-Bromo-1-cyclohexylethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexyl methyl ketone | HCID 13207 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Bromo-1-cyclohexylethanone | HCID 11160027 | 63% |
Reaction Steps
To a solution (50 mL) of 1-cyclohexylethanone (25.0 g) in methanol was added bromine (10.1 mL) at 0° C., and the mixture was stirred at room temperature for 30 min. Saturated sodium sulfite aqueous solution was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (0-10% ethyl acetate/hexane) to give the title object compound (25.8 g, 63%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436043B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-c444b721cc2841e3b4d8d7d224fab347 |
| Source note | uspto-grants-2013_05 |