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HRID 33962作成日:2026年10月24日

Hydrogen Peroxide → 4-Bromoanisole

https://huagongshe.com/ja/reaction/33962

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物Trimethyl borateHCID 8470—
反応物2,4-DibromoanisoleHCID 27011—
反応物ButyllithiumHCID 178418339—
溶媒Acetic AcidHCID 176—
溶媒TetrahydrofuranHCID 8028—
生成物4-BromoanisoleHCID 7730—

反応条件

温度-78 °C

反応手順

In a 500 mL round bottom flask was charged 2,4-dibromoanisole (5.0 g, 18.8 mmol) followed by 200 mL of dry tetrahydrofuran under nitrogen. The reaction mixture was then cooled to −78° C., and n-butyllithium (16.11 mL, 22.56 mmol) was added dropwise. The reaction mixture was stirred for 30 min at −78° C. The reaction mixture was then warmed to 0° C. and trimethylborate (2.57 mL, 22.56 mmol) was added dropwise. The reaction mixture was stirred at room temperature for 30 min. 5 mL of glacial acetic acid was added followed by 10 mL of 35% wt. hydrogen peroxide in a drop wise fashion. The reaction was allowed to stir 12 h at room temperature. The reaction was quenched with 1 N HCl, extracted with ethylacetate (100×3) and the combined organic phases were dried over Na2SO4, filtered and evaporated under reduced pressure. Purification by column chromatography yielded 1 g (26%) of 3-hydroxy, 4-methoxybromobenzene (white crystals). (96:4 Hexanes:ethylacetate).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429681B2
出典データセットuspto-grants-2008_09
ORD IDord-aafb1838a2e14327b1d6510484a2662a
出典メモuspto-grants-2008_09