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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37585생성일: 2026년 10월 23일

Hydrochloric Acid → 2,2-Difluoro-benzo(1,3)dioxole-4-carbaldehyde

https://huagongshe.com/ko/reaction/37585

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DimethylformamideHCID 6228—
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물2,2-Difluoro-1,3-benzodioxoleHCID 74103—
반응물ButyllithiumHCID 178418339—
용매TolueneHCID 1140—
생성물2,2-Difluoro-benzo(1,3)dioxole-4-carbaldehydeHCID 2736970—

반응 단계

94.0 g (272 mmol) of n-butyllithium (18.5% in toluene) are added dropwise under a nitrogen atmosphere, at from -15° to -10° C., over a period of 1.5 hours, to 29.5 g (254 mmol) of N,N,N',N'-tetramethylethylenediamine and 40.0 g (253 mmol) of 2,2-difluoro-1,3-benzodioxole in 35 ml of toluene, an orange suspension being formed. 19.7 g (270 mmol) of DMF are then metered in at from -15° to -10° C. over a period of 1/2 hour. The pale yellow suspension is poured at +10° C. onto 346 g (1.105 mol) of 11.6% aqueous hydrochloric acid and the whole is stirred for 1/2 hour to complete the reaction. The aqueous phase is separated off and the organic phase is concentrated by evaporation in a vacuum rotary evaporator at 50° C./200 mbar under nitrogen to yield the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420301
출처 데이터셋uspto-grants-1995_05
ORD IDord-3eca32ec96e34b94909277e13a1f16e0
출처 메모uspto-grants-1995_05