関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrazine hydrate (1:1) | HCID 24654 | — |
| 反応物 | 2-Fluoro-6-(4-trifluoromethylphenoxy)pyridine | HCID 18544783 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-Hydrazino-6-(4-trifluoromethylphenoxy)pyridine | HCID 18544786 | 47.8% |
反応手順
Next, a reaction flask was loaded with 2-fluoro-6-(4-trifluoromethylphenoxy)pyridine (8.0 g) and ethanol (60 ml), and heated up to 40° C. with stirring. To this mixture, hydrazine monohydrate (7.6 g) was dropwise added in 30 minutes. The temperature of the mixture was raised to the reflux temperature, followed by stirring for 20 hours. Thereafter, the heating was stopped, and the reaction mixture was cooled, followed by filtration to remove insoluble components. The filtrate was condensed by an evaporator to give 2-hydrazino-6-(4-trifluoromethylphenoxy)pyridine (4.0 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06551682B1 |
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| 出典データセット | uspto-grants-2003_04 |
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| ORD ID | ord-172563bbfa8c4f0e8db9a9212f308f10 |
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| 出典メモ | uspto-grants-2003_04 |
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