関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Diethyl (3-oxobutyl)phosphonate | HCID 14033 | — |
| 反応物 | Diethylphosphite | HCID 3780918 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | 4-Acrylamido-4-methyl-2-pentanone | HCID 21584921 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | N-(1,1-Dimethyl-3-oxobutyl)-2-diethylphosphonoacrylamide | HCID 21328247 | 97% |
反応手順
Using the same procedure of Example 1 for the preparation of diethyl 3-oxobutylphosphonate, a solution prepared from the reaction of 3.1 grams (0.135 mole) of sodium with 63 ml of anhydrous ethanol was added under nitrogen and drying conditions with stirring at room temperature to 152 grams (1 mole) of diethyl phosphite. To this solution was then added over a one hour period maintaining the internal temperature at 30°-40° C. with external cooling, 169 grams (1 mole) of diacetone acrylamide. The solution was then stirred for another hour at 24° C. before 8.2 grams (0.135 mole) of acetic acid was slowly added to bring the pH to 5. The solution was dried at 70° C./16 mm and topped off by distillation for 30 minutes with a maximum pot temperature of 120° C. at 0.2 mm. The pot residue (316 grams) was the desired N-(1,1-dimethyl-3-oxybutyl)-2-diethylphosphonoacrylamide in a 97% yield. Structure of the desired product with a purity of about 95% was confirmed by NMR.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04145510 |
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| 出典データセット | uspto-grants-1979_03 |
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| ORD ID | ord-1831c8b74e5a468eb10f888031e8b840 |
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| 出典メモ | uspto-grants-1979_03 |
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