関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Chlorobenzonitrile | HCID 12163 | — |
| 反応物 | n-Butyl lithium | HCID 61028 | — |
| 反応物 | 2-Methylthiazole | HCID 77129 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (Z)-1-(4-chlorophenyl)-2-(thiazol-2-yl)ethenamine | HCID 57750306 | 31% |
反応手順
A 2.5M solution of N-butyllithium (8.00 mL, 20.00 mmol) in hexanes, was added dropwise to 2-methylthiazole (1.983 g, 20 mmol) dissolved in THF (35.00 mL) over a period of 5 minutes under argon at −70° C. The resulting pale yellow slurry was stirred at −70° C. for 2.5 hour. 4-chlorobenzonitrile (2.75 g, 20.00 mmol) in THF (35.00 mL) was added dropwise to the suspension, which was stirred at −70° C. for 90 minutes after the end of the addition. The reaction mixture was allowed to warm to room temperature under stirring and darkened. The crude was concentrated to dryness and diluted with ethyl acetate then washed with water, dried over magnesium sulphate and concentrated. The crude product was purified by flash chromatography on silica gel eluting with 10 to 100% ethyl acetate in dichloromethane. The solvent was evaporated to dryness to afford (Z)-1-(4-chlorophenyl)-2-(thiazol-2-yl)ethenamine (1.466 g, 31.0%) as a pale yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08101623B2 |
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| 出典データセット | uspto-grants-2012_01 |
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| ORD ID | ord-39b6bfe9ef8a414ea5978e6c0eb883e2 |
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| 出典メモ | uspto-grants-2012_01 |
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