HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 1-Bromocyclohexyl 3,5-dimethyl-2-methoxyphenyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Cyclohexyl 3,5-dimethyl-2-methoxyphenyl ketone | HCID 15157169 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-Bromocyclohexyl 3,5-dimethyl-2-methoxyphenyl ketone | HCID 15157172 | — |
Reaction Steps
285.2 Grams of cyclohexyl 3,5-dimethyl-2methoxyphenyl ketone was dissolved in 800 ml of acetic acid. To the solution was added 8 ml of 47% hydrobromic acid and then a solution prepared by dissolving 212 g of bromine in 100 ml of acetic acid was added thereto dropwise with ice-cooling and stirring. After stirring at room temperature for 2 hours, the reaction mixture was poured into ice water, followed by extraction with 2 liters of ethyl acetate. The extract was washed with water and then with a saturated aqueous sodium chloride solution and then dried with anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure to obtain 363.6 g of 1-bromocyclohexyl 3,5-dimethyl-2-methoxyphenyl ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05017724 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-58a8150a4e304f058f0e9d13d38352c8 |
| Source note | uspto-grants-1991_05 |