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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 527657생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/527657

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Trimethyl borateHCID 8470—
반응물Sodium HydroxideHCID 14798—
반응물2,2-Difluoro-1,3-benzodioxoleHCID 74103—
반응물CID 53628100HCID 178418400—
용매TetrahydrofuranHCID 8028—
용매CyclohexaneHCID 8078—
생성물2,2-Difluoro-1,3-benzodioxol-4-olHCID 1111654195.3%

반응 조건

온도-78 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346790B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-83b7b301ea65407dbc620c3fc0d63a85
출처 메모uspto-grants-2016_05