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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719802Generated: October 26, 2026

Benzene, 4-((2-(3-chloro-4-ethoxyphenyl)-2-methylpropoxy)methyl)-1-fluoro-2-phenoxy- → 3-Phenoxytoluene

https://huagongshe.com/reaction/1719802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 4-((2-(3-chloro-4-ethoxyphenyl)-2-methylpropoxy)methyl)-1-fluoro-2-phenoxy-HCID 3068497—
Reactant4-[[2-(4-Ethoxyphenyl)-2-methylpropoxy]methyl]-1-fluoro-2-phenoxybenzeneHCID 15582662—
SolventBenzeneHCID 241—
Product3-PhenoxytolueneHCID 19165—
Product2-(4-Ethoxyphenyl)-2-methylpropanolHCID 158525—

Reaction Steps

The reaction mixture was cooled to room temperature and the gas was released. 100 ml of benzene was charged in the autoclave to dissolve an oil. An insoluble matter was filtered out. After washing with 20 ml of benzene, a resulting mother wash solution was shaken well and then left to stand to obtain a benzene layer. The benzene layer was washed with 100 ml of water three times. Benzene was distilled off under reduced pressure to obtain an oily product. According to gas chromatographic analysis by the internal standard method, the oily product contained 97.2% of 3-phenoxy-4-fluorobenzyl 2-(4-ethoxyphenyl)-2-methylpropyl ether and 1.0% of starting material 3-phenoxy-4-fluorobenzyl 2-(3-chloro-4-ethoxyphenyl)-2-methylpropyl ether. The amounts of 3-phenoxytoluene and 4-ethoxyneophyl alcohol formed by ether bond cleavage were each less than 0.1%. The amount of 3-phenoxybenzyl 2-(4-ethoxyphenyl)-2-methylpropyl ether formed probably due to the replacement of fluorine atom with hydrogen atom was only less than 0.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04542243
Source datasetuspto-grants-1985_09
ORD IDord-c9fca02e170b4588b9d813de5fd80b17
Source noteuspto-grants-1985_09