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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351811Generated: November 2, 2026

Etofenprox → 3-Phenoxytoluene

https://huagongshe.com/reaction/2351811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEtofenproxHCID 71245—
Reactant3-Chloro-4-ethoxyneophyl 3-phenoxybenzyl etherHCID 3067183—
CatalystHCID 178418390HCID 178418390—
Product3-PhenoxytolueneHCID 19165—
Product2-(4-Ethoxyphenyl)-2-methylpropanolHCID 158525—

Reaction Steps

The dechlorination reaction was carried out in the same manner as in Example 1 except that 1.44 g of 10%-palladium-alumina (100% dry) was used instead of the 5%-palladium-carbon used as the hydrogenation catalyst in Example 1, and an oily product was obtained by carrying out the post-treatment in the same manner as in Example 1. 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 97.4% 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 0.7%. The amount of the obtained oily product was 52.0 g and the yield was 93.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873373
Source datasetuspto-grants-1989_10
ORD IDord-ee120250919e49218973cd57aed86b7a
Source noteuspto-grants-1989_10