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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | benzyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate | HCID 19374482 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine | HCID 15279389 | 99.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05424277 |
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| 出典データセット | uspto-grants-1995_06 |
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| ORD ID | ord-e6b45e217a2842468d658089a3c18c68 |
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| 出典メモ | uspto-grants-1995_06 |
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