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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12055Generated: October 27, 2026

Water → 2-Bromo-3-methylcyclohexanone

https://huagongshe.com/reaction/12055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
ReactantSodium AcetateHCID 517045—
ReactantTrimethyl-(3-methyl-cyclohex-1-enyloxy)-silaneHCID 597981—
SolventEthyl AcetateHCID 8857—
SolventOxolane--water (1/1)HCID 21881883—
Product2-Bromo-3-methylcyclohexanoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727979B2
Source datasetuspto-grants-2010_06
ORD IDord-9141ed1670cb49bcba55b96621509c0b
Source noteuspto-grants-2010_06