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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286678Generated: October 27, 2026

Chlorobenzene → Ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoate

https://huagongshe.com/reaction/2286678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantPotassium CarbonateHCID 11430—
Reactantp-(4-(Trifluoromethyl)phenoxy)phenolHCID 170230—
ReactantEthyl 3,4-dibromopentanoateHCID 12922552—
CatalystN,N-Dibutyl-N-ethylbutan-1-aminium bromideHCID 19043781—
SolventWaterHCID 962—
ProductEthyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoateHCID 15692195.2%

Reaction Steps

In a reactor, 15 g of chlorobenzene and 15 g of water were charged, and 12.7 g (0.05 mole) of 4-(4-trifluoromethylphenoxy)phenol, 15.8 g (0.055 mole) of ethyl 3,4-dibromopentanoate and 8.7 g (0.063 mole) of potassium carbonate and 0.3 g (0.001 mole) of tributylethylammonium bromide were added. They were refluxed for 6 hours to react them. The water phase was separated and the organic phase was washed with 5% hydrochloric acid and with water and then, chlorobenzene, ethyl 3,4-dibromopentanoate and low boiling by-products were distilled off at 100° C. under a reduced pressure (0.02-0.05 mmHg) to obtain 18.1 g of ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoate (nD20 1.5175). The yield was 95.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04267317
Source datasetuspto-grants-1981_05
ORD IDord-66aa32489e3a4ccfb619f2bf43f8dfb5
Source noteuspto-grants-1981_05