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HRID 21488作成日:2026年10月26日

benzyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate → 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine

https://huagongshe.com/reaction/21488

反応式

関与物質

役割名称HCID仕込み量
反応物benzyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamateHCID 19374482—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒TolueneHCID 1140—
生成物4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamineHCID 1527938999.6%

反応手順

Benzyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate (2.00 g, 5.51 mmol) synthesized as described above, 5% Pd/C (100 mg) as a catalyst, and toluene (15 ml) as a solvent were charged into a 50 cc round-bottom flask, and the inside of the flask was replaced sufficiently with a hydrogen gas. Then, in a hydrogen gas atmosphere, the mixture was thoroughly stirred for 3 hours at 50° C. After completion of the reaction, the catalyst was separated by filtration, the resulting filtrate was dried with anhydrous magnesium sulfate. After separating the drying agent by filtration, the solvent was distilled off under reduced pressure from the filtrate to obtain quantitatively 2-fluoro-4-chloro-5-cyclopentyloxyaniline (1.26 g) as a pale brown oily substance. The spectral data and the like are shown 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-e6b45e217a2842468d658089a3c18c68
出典メモuspto-grants-1995_06