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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351809Generated: October 31, 2026

Etofenprox → 3-Phenoxytoluene

https://huagongshe.com/reaction/2351809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEtofenproxHCID 71245—
Reactant3-Phenoxybenzyl 2-(3-bromo-4-ethoxyphenyl)-2-methylpropyl etherHCID 15590575—
SolventBenzeneHCID 241—
Product3-PhenoxytolueneHCID 19165—
Product2-(4-Ethoxyphenyl)-2-methylpropanolHCID 158525—

Reaction Conditions

Temperature50 °C

Reaction Steps

The reaction mixture was cooled to 50° C. and the residual pressure was released, and 70 ml of benzene was added into the autoclave to dissolve the oil layer. The catalyst was removed by filtration, and the filtrate was allowed to stand still to cause phase separation to give a benzene layer. Then, the benzene layer was washed with 100 ml of water three times, and benzene was removed by distillation under reduced pressure to give an oily product. From the results of the analysis of oil product by gas chromatography according to the internal standard method, it was found that the oily product comprised 98.6% of 3-phenoxybenzyl 2-(4-ethoxyphenyl)-2-methylpropyl ether and 0.4% of unreacted starting 3-phenoxybenzyl 2-(3-bromo-4-ethoxyphenyl)-2-methylpropyl ether, and that the content of each of 3-phenoxytoluene and 4-ethoxyneophyl alcohol formed by cleaving of the ether linkage was lower than 0.3%. The amount of the obtained oily product was 23.8 g and the yield was 94.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873373
Source datasetuspto-grants-1989_10
ORD IDord-be524b51635741f1abe6fc63a6dbd3b4
Source noteuspto-grants-1989_10