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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280209Generated: October 31, 2026

Hydrochloric Acid → 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone O-(N, N-diethylcarbamoyl)oxime

https://huagongshe.com/reaction/1280209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethylcarbamoyl chlorideHCID 6916—
ReactantTriethylamineHCID 8471—
Reactant5-(2,6-Dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone oximeHCID 86584398—
SolventTetrahydrofuranHCID 8028—
Product5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone O-(N, N-diethylcarbamoyl)oximeHCID 53771053—

Reaction Steps

First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone oxime, 0.12 g of triethylamine, and 10 ml of tetrahydrofuran are placed in a reaction vessel, to which 0.16 g of N,N-diethylcarbamoyl chloride is slowly added dropwise with stirring under ice cooling. After completion of the addition, the reaction mixture is further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone O-(N,N-diethylcarbamoyl)oxime.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448444B1
Source datasetuspto-grants-2002_09
ORD IDord-39bfaac9856c421c8e562844be9840f6
Source noteuspto-grants-2002_09