関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | 4-Chloroaniline | HCID 7812 | — |
| 反応物 | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| 反応物 | 5-Methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-one | HCID 12056392 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 2-(4-Chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-one | HCID 12056399 | 57.8% |
反応手順
5-Methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-one (0.28 g) was mixed with a 1M methylene chloride solution of triethyloxonium tetrafluoroborate (1 ml) at room temperature. The reaction mixture was stirred for 24 hrs at room temperature then p-chloroaniline (0.25 g) in chloroform (10 ml) was added to the mixture at 0° C. The mixture was stirred at room temperature for 1 hr and then water was added. The separated oil was extracted with chloroform. The chloroform layer was dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (chloroform-n-hexane, 1/1) to yield 2-(4-chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-one (0.21 g) having a melting point of 53-54° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06713629B2 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-cd27c9acc26c47ba8554b42114b3e20a |
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| 出典メモ | uspto-grants-2004_03 |
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