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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369658Generated: October 23, 2026

Water → 3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3,3-difluoro-2-propenyloxy)butyloxy)benzene

https://huagongshe.com/en/reaction/369658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium chlorodifluoroacetateHCID 2734985—
Reactant4-(2,6-Dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehydeHCID 53826908—
SolventDiglymeHCID 8150—
Product3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3,3-difluoro-2-propenyloxy)butyloxy)benzeneHCID 2328235716%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1.21 g of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde, 0.87 g of triphenylphosphine and 10 ml of diglyme was stirred at 160° C., to which a solution (5 ml) of 0.69 g of sodium chlorodifluoroacetate in diglyme heated to 60° C. was added dropwise. After stirring at 160° C. for 1.5 hours, the reaction mixture was returned to room temperature, poured into water and extracted twice with 50 ml of diethyl ether. The diethyl ether layers Were combined, washed with water, dried over magnesium sulfate and then concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 0.21 g of 3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3,3-difluoro-2-propenyloxy)butyloxy)benzene (yield, 16%), nD23.0 1.5219.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140274
Source datasetuspto-grants-2000_10
ORD IDord-a67d5650892d4378acaa41ca42f8aa1f
Source noteuspto-grants-2000_10