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HRID 237537作成日:2026年10月25日

4-(4-Bromo-3,5-dimethylphenyl)butan-2-one → 4-(4-Bromo-3,5-dimethylphenyl)-2-methylbutan-2-ol

https://huagongshe.com/reaction/237537

反応式

関与物質

役割名称HCID仕込み量
反応物4-(4-Bromo-3,5-dimethylphenyl)butan-2-oneHCID 86697199—
反応物HCID 178418573HCID 178418573—
溶媒TetrahydrofuranHCID 8028—
溶媒Tetrahydrofuran tolueneHCID 22635083—
生成物4-(4-Bromo-3,5-dimethylphenyl)-2-methylbutan-2-olHCID 86697200—

反応手順

To a solution of 4-(4-bromo-3,5-dimethylphenyl)butan-2-one (100 mg) in tetrahydrofurane (2 mL) is added at 0° C. methylmagnesium bromide (840 μL of a 1.4 M solution in tetrahydrofurane/toluene 1:3). The mixture is stirred for 2 hours while warming to room temperature and then partitioned between saturated aqueous NH4Cl solution and diethylether. The organic phase is dried (MgSO4) and concentrated to give the title compound. Yield: 105 mg; LC (method 8): tR=0.47 min; Mass spectrum (ESI+): m/z=271 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642585B2
出典データセットuspto-grants-2014_02
ORD IDord-a0564b10aa0c429bbf5205f2791e2313
出典メモuspto-grants-2014_02