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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280225Generated: October 30, 2026

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

https://huagongshe.com/reaction/1280225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant4-(Trifluoromethyl)benzaldehydeHCID 67996—
ReactantO-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)hydroxylamine hydrochlorideHCID 18429772—
SolventPyridineHCID 1049—
Product4-(trifluoromethyl)benzaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oximeHCID 5380013595.6%

Reaction Steps

To a mixture of 0.14 g of 4-(trifluoromethyl)benzaldehyde 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 into5% 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 0.37 g (yield, 95.6%) of 4-(trifluoromethyl)benzaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD21.0 1.5387.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448444B1
Source datasetuspto-grants-2002_09
ORD IDord-4db5e12402fe4a5e910febf6d3685267
Source noteuspto-grants-2002_09