HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Bromo-1-cyclohexylethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cyclohexyl methyl ketone | HCID 13207 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Bromo-1-cyclohexylethanone | HCID 11160027 | — |
Reaction Steps
A solution of 5.67 g (45 mmol) cyclohexyl methyl ketone in 27 mL anhydrous methanol was cooled to +10° C. in an ice bath and 9.58 g (60 mmol) bromine was added all at once. The reaction was stirred at +10° C. for 45 minutes, upon which time 7.5 mL of water was added. The reaction was stirred at room temperature for a further 2.5 hr and concentrated. The crude product was taken up in ether and washed with brine. The organic phase was dried over MgSO4 and concentrated to afford crude 2-bromo-1-cyclohexyl-ethanone. The product was used immediately in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07488832B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-cabd04cff02b493f931c3ebe132dae9c |
| Source note | uspto-grants-2009_02 |