戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1664707作成日:2026年10月26日

Pyridine → Methyl (S)-4,4-difluoro-2-isocyanatopentanoate

https://huagongshe.com/reaction/1664707

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物TolueneHCID 1140—
反応物PhosgeneHCID 6371—
反応物Methyl (S)-2-amino-4,4-difluoropentanoate hydrobromideHCID 86635602—
溶媒DichloromethaneHCID 6344—
生成物Methyl (S)-4,4-difluoro-2-isocyanatopentanoateHCID 5794624394%

反応条件

温度0 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08039480B2
出典データセットuspto-grants-2011_10
ORD IDord-a3a361f6b17846f0af2217a34ebedc7f
出典メモuspto-grants-2011_10