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HRID 30754作成日:2026年10月24日

Ethanol → 2-(4-Bromo-2,6-dimethylphenoxy)ethanol

https://huagongshe.com/ja/reaction/30754

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物TetrahydrofuranHCID 8028—
反応物Ethyl (4-bromo-2,6-dimethylphenoxy)acetateHCID 875019—
反応物Sodium borohydrideHCID 4311764—
溶媒WaterHCID 962—
生成物2-(4-Bromo-2,6-dimethylphenoxy)ethanolHCID 5370744397.6%

反応手順

Sodium borohydride (0.21 g) was added to a mixture of ethyl (4-bromo-2,6-dimethylphenoxy)acetate (0.78 g), tetrahydrofuran (5 mL) and ethanol (5 mL), and the mixture was stirred at room temperature for 4 hrs. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent:ethyl acetate/n-hexane=1/2) to afford the title compound (0.65 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423185B2
出典データセットuspto-grants-2008_09
ORD IDord-63919e776b274c8f99d5d3eca09608aa
出典メモuspto-grants-2008_09