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HRID 1383750作成日:2026年10月27日
Potassium Iodide → Phosphoric Acid di-tert-butyl Ester 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl Ester
https://huagongshe.com/reaction/1383750
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-(Chloromethyl)-5,5-diphenylimidazolidine-2,4-dione | HCID 11098633 | — |
| 反応物 | Potassium di-tert-butyl phosphate | HCID 23674467 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | Phosphoric Acid di-tert-butyl Ester 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl Ester | HCID 15459545 | 38.6% |
反応手順
35.5 Grams of 3-(chloromethyl)-5,5-diphenyl-2,4-imidazolidinedione from Step (A), 30.7 g of potassium di(t-butyl) phosphate, 0.6 g of potassium carbonate, and 0.15 g of potassium iodide were slurried into 200 mL acetonitrile. The reaction mixture was heated at reflux for 2.5 hours. The solution was filtered to remove potassium chloride precipitate. The filtrate was cooled to 0° C. and filtered to give 22.3 g of the title compound (38.6% yield); mp 108.5° C. (d). 1H NMR (DMSO-d6): 1.3 ppm (s, 18H), 5.2 (d, 2H), 7.3-7.5 (m, 10H), 9.9 (s, 1H); doublet from long range phosphorus coupling.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06255492B1 |
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| 出典データセット | uspto-grants-2001_07 |
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| ORD ID | ord-92da913ed7284ceca65d24fa3ae26c6d |
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| 出典メモ | uspto-grants-2001_07 |
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