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HRID 432221作成日:2026年10月25日

3-Phenoxybenzyl alcohol → (2-Bromo-5-phenoxyphenyl)methanol

https://huagongshe.com/reaction/432221

反応式

関与物質

役割名称HCID仕込み量
反応物3-Phenoxybenzyl alcoholHCID 26295—
反応物N-bromobutanimideHCID 67184—
溶媒AcetonitrileHCID 6342—
生成物(2-Bromo-5-phenoxyphenyl)methanolHCID 2234675885%

反応手順

To a solution of 3-phenoxyphenyl methanol (4.0 g, 0.020 mol) in anhydrous acetonitrile was added 1-bromo-2,5-pyrrolidinedione (3.73 g, 0.021 mol) at room temperature. The mixture was stirred at room temperature for one and a half hour under an atmosphere of nitrogen. The solvents were removed under the reduced pressure. Tetrachloromethane (100 mL) was added to the residue, and the mixture was filtered. The filtrate was concentrated into the residue, and the residue was purified by flash chromatography on silica gel using ethyl acetate/n-heptane (1:5) as mobile phase to yield (2-bromo-5-phenoxyphenyl)methanol (4.7 g, 0.017 mol): RP-HPLC (Hypersil C18, 5 μm, 250×4.6 mm; 25%-100% over 10 min with 0.1 M ammonium acetate, 1 mL/min) Rt 11.7 min. TLC (ethyl acetate/heptane 1:5) Rf 0.18.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06660744B1
出典データセットuspto-grants-2003_12
ORD IDord-e6881106d19a47819921a3fd29407149
出典メモuspto-grants-2003_12