HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Bromo-1-cyclohexylethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Cyclohexyl methyl ketone | HCID 13207 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-1-cyclohexylethanone | HCID 11160027 | 100% |
Reaction Steps
Cyclohexyl methyl ketone (0.30 mL, 2.4 mmol) [Alfa Aesar cat#L05501] was dissolved in methanol (3.0 mL, 74 mmol) cooled in an ice bath and bromine (0.38 g, 2.4 mmol) was added drop wise. The mixture was stirred for 2 h and then water (3.0 mL) was added and the reaction mixture was allowed to stir for 4 h. The reaction mixture was extracted with EtOAc:hexane (3:1). The combined organic layer was washed with water saturated potassium carbonate, brine, dried over magnesium sulfate and concentrated to give as 2-bromo-1-cyclohexylethanone as a clear oil (0.49 g, 100%). 1H NMR (300 MHz, CDCl3) δ 3.96 (s, 2H), 2.86-2.55 (m, 1H), 2.24-1.08 (m, 10H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09227985B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-79485f0eda3f40e89860d8e2022f5de5 |
| Source note | uspto-grants-2016_01 |