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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351808Generated: October 31, 2026

Etofenprox → 3-Phenoxytoluene

https://huagongshe.com/reaction/2351808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEtofenproxHCID 71245—
Reactant3-Chloro-4-ethoxyneophyl 3-phenoxybenzyl etherHCID 3067183—
SolventBenzeneHCID 241—
Product3-PhenoxytolueneHCID 19165—
Product2-(4-Ethoxyphenyl)-2-methylpropanolHCID 158525—

Reaction Steps

The reaction mixture was cooled to room temperature and the residual pressure was released, and 120 ml of benzene was added into the autoclave to dissolve the oil layer. Then, the insoluble substance was removed by filtration, and the mother liquid was washed with 30 ml of benzene, sufficiently shaken and allowed to stand still to cause phase separation and give a benzene layer. The benzene layer was washed with 120 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 the oily product by gas chromatography according to the internal standard method, it was found that the oily product comprised 98.5% of 3-phenoxybenzyl 2-(4-ethoxyphenyl)-2-methylpropyl ether and 0.5% of unreacted starting 3-phenoxybenzyl 2-(3-chloro-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 53.6 g and the yield was 96.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873373
Source datasetuspto-grants-1989_10
ORD IDord-f9ecd808af524dcf8801503ac4ddf198
Source noteuspto-grants-1989_10