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HRID 27357作成日:2026年10月26日

Phenylacetone → Oxindole

https://huagongshe.com/reaction/27357

反応式

関与物質

役割名称HCID仕込み量
反応物PhenylacetoneHCID 7678—
反応物1-amino-1,3-dihydro-2H-indol-2-oneHCID 3775366—
生成物OxindoleHCID 321710—

反応手順

U.S. Pat. Nos. 4,045,576 and 4,126,635 disclose methods for the preparation of 7-benzoylindolin-2-ones. According to one method, 1-aminoindolin-2-one is reacted with a phenylacetone to give a 1-(α-methylphenethylindenimino) indolin-2-one which is cyclized in ethanolic hydrogen chloride to an ethyl α-(2-methyl-3-phenylindol-7-yl)acetate. This indolylester is treated with ozone in acetic acid solution to give an ethyl 2-acetamido-3-benzoylphenylacetate which is hydrolyzed and cyclized in dilute mineral acid to a 7-benzoylindolin-2-one.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04221716
出典データセットuspto-grants-1980_09
ORD IDord-1af7a583fb2c48e7b4214560c751454d
出典メモuspto-grants-1980_09