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HRID 527657作成日:2026年10月26日

Hydrogen Peroxide → 2,2-Difluoro-1,3-benzodioxol-4-ol

https://huagongshe.com/reaction/527657

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Sodium HydroxideHCID 14798—
反応物2,2-Difluoro-1,3-benzodioxoleHCID 74103—
反応物CID 53628100HCID 178418400—
溶媒TetrahydrofuranHCID 8028—
溶媒CyclohexaneHCID 8078—
生成物2,2-Difluoro-1,3-benzodioxol-4-olHCID 1111654195.3%

反応条件

温度-78 °C

反応手順

2,2-Difluoro-1,3-benzodioxole (320 mg, 2.05 mmol) was dissolved in THF (2.5 mL) and cyclohexane (1.2 mL) and the resulting solution cooled down to −78° C. sec-BuLi 2M solution in cyclohexane (1.025 ml, 2.05 mmol) was added drop wise and the reaction mixture stirred for 2 hours at −78° C. Trimethylborate (230 mg, 2.25 mmol) was added and the mixture was allowed to warm slowly to room temperature. A 30% w/w aqueous solution of H2O2 (4.1 mmol) and NaOH (82 mg, 2.05 mmol) were added and the reaction mixture stirred for 18 hours at room temperature. The reaction was quenched with a 2N aqueous solution of HCl and diluted with ethyl acetate. Two phases were separated and the organic layer was washed twice with brine, dried over Na2SO4 and evaporated to dryness, affording the title compound (340 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09346790B2
出典データセットuspto-grants-2016_05
ORD IDord-83b7b301ea65407dbc620c3fc0d63a85
出典メモuspto-grants-2016_05