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Hydrochloric Acid → Methyl 2-cyano-3-(3,4-dichloro-5-isothiazolyl)-3-oxopropanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Methyl cyanoacetate | HCID 7747 | — |
| 反応物 | 3,4-Dichloro-5-isothiazolecarbonyl chloride | HCID 10976886 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Methyl 2-cyano-3-(3,4-dichloro-5-isothiazolyl)-3-oxopropanoate | HCID 12115370 | 84.8% |
反応手順
To a solution of methyl cyanoacetate (1.98 g) in unhydrous tetrahydrofuran (20 ml) 60% sodium hydride (1.6 g) was added at a temperature below 10° C. To the reaction mixture a solution of 3,4-dichloro-5-isothiazolecarbonyl chloride (4.30 g) in unhydrous tetrahydrofuran (15 ml) was added dropwise at the same temperature. After finishing the addition, the reaction mixture was stirred at room temperature for 2 hours and 1N-aqueous hydrochloric acid (10 ml) was added. After extraction with ethyl acetate and drying the organic phase with unhydrous sodium sulfate, the solvent was distilled off under reduced pressure to obtain methyl 2-cyano-3-(3,4-dichloro-5-isothiazolyl)-3-oxopropanoate (4.7 g) as pale yellow crystals. mp 119-122° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06706748B2 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-9ff7649d71484e3191a1ce31b2bc2cba |
| 出典メモ | uspto-grants-2004_03 |