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HRID 1280239생성일: 2026년 10월 24일

Triphenylphosphine → 3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene

https://huagongshe.com/ko/reaction/1280239

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물4-(3,3-Dichloro-2-propenyloxy)-2,6-dichlorophenolHCID 11346738—
반응물4-(2,2-Diethoxyethoxy)butanolHCID 18430111—
용매TetrahydrofuranHCID 8028—
생성물3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzeneHCID 1842939392.1%

반응 단계

To a mixture of 2.30 g of 4-(2,2-diethoxyethoxy)butanol, 2.94 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 2.94 g of triphenylphosphine, and 30 ml of tetrahydrofuran was slowly added dropwise 2.48 g of diisopropylazodicarboxylate with stirring in a stream of nitrogen gas under ice cooling. After stirring at room temperature for 24 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 4.48 g (yield, 73%) of 3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06448444B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-11a63c19d8ce410f821be956da910c78
출처 메모uspto-grants-2002_09