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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 859846생성일: 2026년 10월 26일

Hydrogen Peroxide → 1H-Isophosphindole, 2-(1,1-dimethylethyl)-2,3-dihydro-, 2-oxide

https://huagongshe.com/reaction/859846

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물tert-ButylphosphineHCID 123165—
반응물1,5-Dihydro-benzo[e][1,3,2]dioxathiepine 3,3-dioxideHCID 11117056—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1H-Isophosphindole, 2-(1,1-dimethylethyl)-2,3-dihydro-, 2-oxideHCID 1143571694%

반응 단계

To a solution of tert-butyl phosphine (1.40 mL, 11.5 mmol) in THF (40 mL) was added dropwise n-BuLi (11.5 mmol) at −78° C. The resulting yellow solution was allowed to warm to rt and stirred at rt for 1 h. A solution of 40 (2.29 g, 11.5 mmol) in THF (20 mL) was added at −78° C. via cannula. The resulting solution was allowed to warm to rt and stirred at rt for 5 h. After being cooled to −78° C. again, n-BuLi (11.5 mmol) was added dropwise. The reaction mixture was warmed to rt and stirred overnight. 2.5 mL H2O2 (30% aq.) was added at 0° C. After being stirred at 0° C. for 1 h, the reaction was quenched with saturated Na2SO3 solution (10 mL) at 0° C. for 1 h. After usual workup, the crude product was purified by recrystallization (CH2Cl2 and hexane) to give 50 as white crystals (2.26 g, 94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07153809B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-008eec4e04014a55980bf6a7c5569126
출처 메모uspto-grants-2006_12