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HRID 2358866作成日:2026年10月25日
Hydrochloric Acid → N-(1,1-Dimethyl-2-methylthioethyl)-N'-[2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]phthalamide
https://huagongshe.com/reaction/2358866
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Methyl chloroformate | HCID 6586 | — |
| 反応物 | Phthalic Anhydride | HCID 6811 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 4-(1,1,1,2,3,3,3-Heptafluoropropan-2-yl)-2-methylaniline | HCID 9925543 | — |
| 反応物 | N-[1,1-dimethyl-2-(methylthio)ethyl]phthalamic acid | HCID 11437082 | — |
| 反応物 | 2-Propanamine, 2-methyl-1-(methylthio)- | HCID 12097380 | — |
| 溶媒 | 1,2-Dichloroethane | HCID 11 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | N-(1,1-Dimethyl-2-methylthioethyl)-N'-[2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]phthalamide | HCID 22066226 | 92% |
反応手順
A mixture of 2-methyl-1-methylthio-2-propanamine (11.61 g) and triethylamine (1.97 g) was added dropwise to a mixture of phthalic anhydride (14.42 g) and 1,2-dichloroethane (58 mL) at 50° C. The resulting mixture was stirred at the same temperature for 30 minutes to prepare N-[1,1-dimethyl-2-(methylthio)ethyl]phthalamic acid. Aqueous sodium hydrogencarbonate solution (9.81 g/101 mL) was added dropwise to this mixture at 40° C. and then methyl chloroformate (11.04 g) was added dropwise thereto at the same temperature. After completion of the dropwise addition, the reaction mixture was stirred at 50° C. for 1 hour and the organic layer was separated to prepare a solution of N-[1,1-dimethyl-2-(methylthio)ethyl]isophthalimide in 1,2-dichloroethane. This solution was added dropwise to a mixture of 2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoro-methyl)ethyl]aniline (25.45 g), concentrated hydrochloric acid (0.49 g) and 1,2-dichloroethane (14.4 mL) at 60° C., and then stirred at 65° C. for 30 minutes. The reaction mixture was cooled and then neutralized with an aqueous sodium hydrogencarbonate solution, after which the organic layer was separated. The organic layer obtained was concentrated under reduced pressure, and the crystals precipitated were filtered, washed with water and then dried to obtain 47.06 g (yield 92%) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07763750B2 |
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| 出典データセット | uspto-grants-2010_07 |
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| ORD ID | ord-6524f59788c141b3b9e38fde66526570 |
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| 出典メモ | uspto-grants-2010_07 |
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