関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Phosgene | HCID 6371 | — |
| 反応物 | Methyl (S)-2-amino-4,4-difluoropentanoate hydrobromide | HCID 86635602 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Methyl (S)-4,4-difluoro-2-isocyanatopentanoate | HCID 57946243 | 94% |
反応手順
The compound from example 6 (6.76 g, 28.8 mmol) was initially charged and dissolved in 240 ml of dichloromethane and 9.46 ml (117 mmol, 4.05 eq) of pyridine, cooled down to 0° C. in an ice bath for 15 min and admixed with 19.86 ml of a 20% phosgene solution in toluene (37.54 mmol, 1.3 eq) within 20-30 seconds. The mixture was stirred at 0° C. for a further 2 h, then the reaction mixture was extracted with cold half-molar HCl and ice. The water phases were reextracted with dichloromethane, and the combined organic phases were washed with ice and saturated NaCl solution, then dried over MgSO4 and filtered off from the desiccant. Concentration by evaporation under reduced pressure left 5.21 g of brown oil (corresponded to a yield of 94%), which was reacted further directly.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08039480B2 |
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| 出典データセット | uspto-grants-2011_10 |
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| ORD ID | ord-a3a361f6b17846f0af2217a34ebedc7f |
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| 出典メモ | uspto-grants-2011_10 |
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