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HRID 21475作成日:2026年10月26日

2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzene → 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine

https://huagongshe.com/reaction/21475

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzeneHCID 19374470—
触媒HCID 178418390HCID 178418390—
溶媒TolueneHCID 1140—
生成物4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamineHCID 15279389—

反応手順

The resulting 2-fluoro-4-chloro-5-cyclopentyloxynitrobenzene (13.0 g, 50.1 mmol) was dissolved in toluene (100 ml), a catalytic amount of 10% palladium-carbon (0.5 g) was added thereto, and the mixture was reacted at room temperature to 70° C. under a hydrogen pressure of 3 to 5 atms. in a glass autoclave. After absorption of hydrogen gas ceased, the catalyst was removed by filtration, and the solvent was distilled off under reduced pressure from the filtrate to obtain substantially quantitatively oily 2-fluoro-4-chloro-5-cyclopentyloxyaniline. The spectral data and the like are as described in Reference Example 1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05424277
出典データセットuspto-grants-1995_06
ORD IDord-67f78207c5b64f1ab0a8cb7a7aad0bee
出典メモuspto-grants-1995_06