関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium Chloride | HCID 5234 | — |
| 反応物 | Diethyl Oxalate | HCID 7268 | — |
| 反応物 | Potassium thiocyanate | HCID 516872 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | ethyl 2-(N-phenylformamido)acetate | HCID 14416604 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | HCID 178470333 | HCID 178470333 | 48% |
反応手順
Absolute ethanol (50 mL) was slowly added to a mechanically stirred suspension of finely cut sodium metal (19.3 g; 0.84 mol) in anhydrous ether (500 mL). When most of the metal had dissolved, diethyl oxalate (114 mL; 0.84 mol) was slowly added followed by the slow addition of the N-phenyl-N-formylglycine ethyl ester (130 g; 0.67 mol). The mixture was stirred at room temperature overnight and then ice-water (700 mL) was added. The resulting emulsion was broken by sequential addition of a saturated sodium chloride solution (150 mL) and water (200 mL). The aqueous layer was removed, potassium thiocyanate (114 g; 1.18 mol) was added, then concentrated hydrochloric acid (160 mL), followed by absolute ethanol (900 mL). The resultant mixture was warmed at 60°-65° C. for 1 hour, then at 50° C. for 6 hours and finally allowed to stir at room temperature overnight. The light yellow precipitate was filtered, washed with ethanol and dried to give 103 g (48%) of diethyl 2-mercapto-1-phenyl-4,5-imidazoledicarboxylate (mp 145°-146° C.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05329012 |
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| 出典データセット | uspto-grants-1994_07 |
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| ORD ID | ord-1706884c5fd742b48f17201e467f3009 |
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| 出典メモ | uspto-grants-1994_07 |
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