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HRID 26271作成日:2026年10月24日

Oxygen → 1-phenyl-1H-pyrazol-3-amine

https://huagongshe.com/ja/reaction/26271

反応式

関与物質

役割名称HCID仕込み量
反応物OxygenHCID 977—
反応物PyridineHCID 1049—
反応物3-Amino-1-phenylpyrazoleHCID 98736—
触媒CopperHCID 23978—
溶媒EthanolHCID 702—
生成物1-phenyl-1H-pyrazol-3-amineHCID 594320—

反応手順

1-phenyl-3-amino-2-pyrazoline, copper salt (CuCl) and metallic copper, if any, and/or pyridine, in the form of a suspension or of a solution in the solvent (e.g., ethyl alcohol) are introduced, in the desired amounts (between 5 and 6%), into a reactor equipped with feeding systems for reagents and with an effective stirrer. Stirring is started in an oxygen atmosphere. After about 2 hours, oxidation is concluded and the whole solid is dissolved. The catalyst is filtered, the solvent is distilled under vacuum, and the 1-phenyl-3-aminopyrazole is isolated by extraction with, e.g., n-heptane. Additional 1-phenyl-3-aminopyrazole is recovered by treating the n-heptane extraction residue with diluted hydrochloric acid, followed by neutralization with aqueous NaOH to precipitate the 1-phenyl-3-aminopyrazole. Optionally, the heptane extraction residue diluted with hydrochloric acid can be clarified with animal charcoal, prior to neutralization thereof. As is known, the 1-phenyl-3-aminopyrazoles are an important class of products which are valuable for various industrial uses, such as active intermediates in the preparation of dyestuffs, of sensitive agents for use in photography, and of other fine chemicals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04149005
出典データセットuspto-grants-1979_04
ORD IDord-9a092b14e4bf42dcacfaef1c825897eb
出典メモuspto-grants-1979_04