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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 369660생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/369660

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물1,1,1-Trichloro-2,2,2-trifluoroethaneHCID 9635—
반응물5-(2,6-Dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehydeHCID 54045208—
촉매ZincHCID 23994—
용매DimethylformamideHCID 6228—
생성물(Z)-3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(5-(3-chloro-4,4,4-trifluoro-2-butenyloxy)pentyloxy)benzeneHCID 8675596614%

반응 단계

To a mixture of 1.21 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehyde, 0.57 g of zinc dust and 10 ml of N,N-dimethylformamide was added 0.82 g of 1,1,1-trichlorotrifluoroethane. After stirring at room temperature for 1.5 hours, 0.44 g of acetic anhydride was added. The reaction mixture was stirred at room temperature for 3 hours and then filtered. The filtrate was poured into 20 ml of diluted hydrochloric acid and extracted twice with 50 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 0.21 g of (Z)-3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(5-(3-chloro-4,4,4-trifluoro-2-butenyloxy)pentyloxy)benzene [the integrated CF3 signal ratio of Z/E=94/6 as determined by 19F-NMR (CDCl3 /CFCl3)] (yield, 14%), nD26.5 1.5123.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06140274
출처 데이터셋uspto-grants-2000_10
ORD IDord-ea00d6a1397d483481fa7f3186c5f968
출처 메모uspto-grants-2000_10