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HRID 12055作成日:2026年10月25日

Water → 2-Bromo-3-methylcyclohexanone

https://huagongshe.com/reaction/12055

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物N-bromobutanimideHCID 67184—
反応物Sodium AcetateHCID 517045—
反応物Trimethyl-(3-methyl-cyclohex-1-enyloxy)-silaneHCID 597981—
溶媒Ethyl AcetateHCID 8857—
溶媒Oxolane--water (1/1)HCID 21881883—
生成物2-Bromo-3-methylcyclohexanoneHCID 21541956—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727979B2
出典データセットuspto-grants-2010_06
ORD IDord-9141ed1670cb49bcba55b96621509c0b
出典メモuspto-grants-2010_06