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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 369669생성일: 2026년 10월 24일

Acetic Anhydride → (Z)-3,5-diethyl-1-(3,3-dichloro-2-propenyloxy)-4-(5-(3-chloro-4,4,4-trifluoro-2-butenyloxy)pentyloxy)benzene

https://huagongshe.com/ko/reaction/369669

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물1,1,1-Trichloro-2,2,2-trifluoroethaneHCID 9635—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물5-(2,6-Diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehydeHCID 53738776—
촉매ZincHCID 23994—
용매DimethylformamideHCID 6228—
생성물(Z)-3,5-diethyl-1-(3,3-dichloro-2-propenyloxy)-4-(5-(3-chloro-4,4,4-trifluoro-2-butenyloxy)pentyloxy)benzeneHCID 86755968192.5%

반응 단계

To a mixture of 0.12 g of aluminum chloride and 50 ml of N,N-dimethylformamide was added 3.04 g of 1,1,1-trichlorotrifluoroethane. After stirring at room temperature for 1 hour, 1.21 g of 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehyde was added, and the reaction mixture was further stirred at room temperature for 4 hours, to which 1.38 g of acetic anhydride was added. After stirring at room temperature for 1 hour, 0.88 g of zinc dust was added, and the reaction mixture was stirred at room temperature for 12 hours and filtered. The filtrate was poured into 50 ml of diluted hydrochloric acid and extracted twice with 100 ml of diethyl ether. The diethyl ether layers were combined, washed with water, dried over magnesium sulfate and then evaporated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 2.91 g of (Z)-3,5-diethyl-1-(3,3-dichloro-2-propenyloxy)-4-(5-(3-chloro-4,4,4-trifluoro-2-butenyloxy)pentyloxy)benzene (yield, 72%), nD26.0 1.4958.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06140274
출처 데이터셋uspto-grants-2000_10
ORD IDord-e8a7db0a2be54d9580a7dbbfe22b336d
출처 메모uspto-grants-2000_10