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HRID 267469作成日:2026年10月27日

Perylene → 3-Perylenecarboxaldehyde

https://huagongshe.com/reaction/267469

反応式

関与物質

役割名称HCID仕込み量
反応物PeryleneHCID 9142—
反応物Phosphorus oxychlorideHCID 24813—
反応物N-MethylformanilideHCID 66737—
反応物Sodium AcetateHCID 517045—
溶媒WaterHCID 962—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物3-PerylenecarboxaldehydeHCID 3698916—

反応手順

About 22 grams N-methylformanilide is initially dissolved in 40 milliliters o-dichlorobenzene, the vessel containing the above solution partially immersed in a water bath (bath temperature less than 25° C) and 22 grams phosphorous oxychloride introduced into the flask by dropewise addition. About 20 grams of perylene is stirred into the above solution and the resulting mixture heated on a steam bath for twelve hours (temperature of contents of vessel 90°-95° C). The contents of the flask are thereafter poured into a second vessel containing 100 grams sodium acetate dissolved in 250 milliliters water. The organic liquid phase of the mixture is separated from the aqueous phase by steam distillation. Crude aldehyde is thereafter precipitated from aqueous solution and the solids recystalized from acetic acid and from benzene. The solids thus obtained are further extracted in a soxhlet extractor with 30-60 pet ether. The material remaining in the extraction thimble is 3-perylenecarboxaldehyde, mp 230° C; yield 9.5 grams.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03943108
出典データセットuspto-grants-1976_03
ORD IDord-208a3fab508844b2a70188954870e1fd
出典メモuspto-grants-1976_03