Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2351806Erstellt: 26. Oktober 2026

Etofenprox → 3-Phenoxytoluene

https://huagongshe.com/reaction/2351806

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEtofenproxHCID 71245—
Edukt3-Chloro-4-ethoxyneophyl 3-phenoxybenzyl etherHCID 3067183—
LösungsmittelBenzeneHCID 241—
Produkt3-PhenoxytolueneHCID 19165—
Produkt2-(4-Ethoxyphenyl)-2-methylpropanolHCID 158525—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

The reaction mixture was cooled to 50° C. and the residual pressure was released, and 100 ml of benzene was added into the autoclave to dissolve the oil layer. Then, the catalyst was removed by filtration, and the filtrate was allowed to stand still to cause phase separation, and the benzene layer was recovered and 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 98.8% of 3-phenoxybenzyl 2-(4-ethoxyphenyl)-2-methylpropyl ether and 0.3% 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 53.8 g, and the yield was 96.7%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04873373
Quelldatensatzuspto-grants-1989_10
ORD IDord-413d38bb0cd042b7b6e224623631a215
Quellennotizuspto-grants-1989_10