HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Bromo-3-methylcyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Trimethyl-(3-methyl-cyclohex-1-enyloxy)-silane | HCID 597981 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 2-Bromo-3-methylcyclohexanone | HCID 21541956 | — |
Reaction Steps
A solution of N-bromosuccinimide (0.48 mmol) and sodium acetate (0.04 mmol) in THF/water (1:1, 5.2 ml) is cooled to 0° C. and trimethyl-(3-methyl-cyclohex-1-enyloxy)-silane (0.4 mmol, 80% pure) is added dropwise. The reaction mixture is heated to room temperature and stirring is continued overnight. After addition of water extraction is carried out with ethyl acetate. The title compound is obtained from the combined organic phases after drying over sodium sulphate and evaporating-off of the solvent in a vacuum (JOC 1997, 62, 19, 6692-6696).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07727979B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-9141ed1670cb49bcba55b96621509c0b |
| Source note | uspto-grants-2010_06 |