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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 369667생성일: 2026년 10월 24일

1,1,1-Trichloro-2,2,2-trifluoroethane → 3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3,3-dichloro-4,4,4-trifluoro-2-hydroxybutyloxy)butyloxy)benzene

https://huagongshe.com/ko/reaction/369667

반응식

참여 물질

역할이름HCID투입량
반응물1,1,1-Trichloro-2,2,2-trifluoroethaneHCID 9635—
반응물4-(2,6-Dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehydeHCID 53826908—
촉매ZincHCID 23994—
용매DimethylformamideHCID 6228—
생성물3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3,3-dichloro-4,4,4-trifluoro-2-hydroxybutyloxy)butyloxy)benzeneHCID 2328241363.4%

반응 단계

To a mixture of 2.01 g of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde, 1.31 g of zinc dust and 10 ml of N,N-dimethylformamide was added 4.12 g of 1,1,1-trichlorotrifluoroethane. After stirring at room temperature for 1.5 hours, the reaction mixture was filtered. The filtrate was poured into 20 ml of diluted hydrochloric acid and extracted twice with 50 ml of ethyl acetate. The ethyl acetate 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 1.76 g of 3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3,3-dichloro-4,4,4-trifluoro-2-hydroxybutyloxy)butyloxy)benzene (yield, 63%), nD24.2 1.5188.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06140274
출처 데이터셋uspto-grants-2000_10
ORD IDord-0618dde99335441b96a472b8e46bca52
출처 메모uspto-grants-2000_10