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HRID 1280226생성일: 2026년 10월 26일

Citric Acid → 4'-(trifluoromethyl)acetophenone O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime

https://huagongshe.com/reaction/1280226

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물1-(4-(Trifluoromethyl)phenyl)ethan-1-oneHCID 69731—
반응물O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)hydroxylamine hydrochlorideHCID 18429772—
용매PyridineHCID 1049—
생성물4'-(trifluoromethyl)acetophenone O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oximeHCID 5445311275.5%

반응 단계

To a mixture of 0.15 g of 4′-(trifluoromethyl)acetophenone and 10 ml of pyridine was added 0.30 g of O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into 5% aqueous citric acid solution, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.30 g (yield, 75.5%) of 4′-(trifluoromethyl)acetophenone O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD21.5 1.5420.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06448444B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-e6027f50ed44487c8eeadf671f8d2a4a
출처 메모uspto-grants-2002_09