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HRID 1719801作成日:2026年10月25日

Etofenprox → 3-Phenoxytoluene

https://huagongshe.com/reaction/1719801

反応式

関与物質

役割名称HCID仕込み量
反応物EtofenproxHCID 71245—
反応物3-Phenoxybenzyl 2-(3-bromo-4-ethoxyphenyl)-2-methylpropyl etherHCID 15590575—
溶媒BenzeneHCID 241—
生成物3-PhenoxytolueneHCID 1916598%

反応手順

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 98.5% of intended 3-phenoxybenzyl 2-(4-ethoxyphenyl)-2-methylpropyl ether and 0.3% of starting material 3-phenoxybenzyl 2-(3-bromo-4-ethoxyphenyl)-2-methylpropyl ether. The amounts of 3-phenoxytoluene and 4-ethoxyneophy alcohol formed by ether bond cleavage were each less than 0.2%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04542243
出典データセットuspto-grants-1985_09
ORD IDord-e2d07f91bbe94da086a7ca76b3f85d06
出典メモuspto-grants-1985_09