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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 369668생성일: 2026년 10월 23일

Hydrochloric Acid → 3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3-cyano-3,3-dichloro-2-hydroxypropyloxy)butyloxy)benzene

https://huagongshe.com/ko/reaction/369668

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TrichloroacetonitrileHCID 11011—
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-cyano-3,3-dichloro-2-hydroxypropyloxy)butyloxy)benzeneHCID 23282423246.7%

반응 단계

To a mixture of 0.60 g of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde, 0.29 g of zinc dust and 10 ml of N,N-dimethylformamide was added 0.040 g of trichloroacetonitrile with stirring at room temperature. After stirring at room temperature for 2 hours, the reaction mixture was poured into 10 ml of diluted hydrochloric acid and extracted twice with 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 0.35 g of 3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3-cyano-3,3-dichloro-2-hydroxypropyloxy)butyloxy)benzene (yield, 46%), nD24.0 1.5460.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06140274
출처 데이터셋uspto-grants-2000_10
ORD IDord-a5f3b8803f37432985d69c929f857358
출처 메모uspto-grants-2000_10