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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363086Generated: October 30, 2026

Potassium Carbonate → 3-Chloro-4-[3-(4-trifluoromethylphenoxy) propyloxy]-5-methyl-1-(3,3-dichloro-2-propenyloxy)benzene

https://huagongshe.com/reaction/363086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, 1-(3-bromopropoxy)-4-(trifluoromethyl)-HCID 11781023—
Reactant1-(3-Bromopropoxy)-4-(trifluoromethoxy)benzeneHCID 13672275—
Reactant2-Chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenolHCID 18504695—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product3-Chloro-4-[3-(4-trifluoromethylphenoxy) propyloxy]-5-methyl-1-(3,3-dichloro-2-propenyloxy)benzeneHCID 5380305294.9%

Reaction Steps

First, 0.35 g of 1-(3-bromopropyloxy)-4-trifluoromethylbenzene (prepared in the same manner as described above for 1-(3-bromopropyloxy)-4-trifluoromethoxybenzene) and 0.2 g of potassium carbonate were dissolved in 100 ml of N,N-dimethylformamide, to which 0.3 g of 2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenol was added, and the mixture was stirred at room temperature for 24 hours. The reaction mixture was mixed with 200 ml of diethyl ether, washed with water, dried with anhydrous magnesium sulfate, and concentrated to obtain a crude product. The crude product was subjected to silica gel chromatography, which afforded 0.50 g of 3-chloro-4-[3-(4-trifluoromethylphenoxy) propyloxy]-5-methyl-1-(3,3-dichloro-2-propenyloxy)benzene (94% yield), nD23.0 1.5330.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872137
Source datasetuspto-grants-1999_02
ORD IDord-ea71162892f44dcabd4cc1a971eff7e4
Source noteuspto-grants-1999_02