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HRID 1972生成日期:2026年10月23日

碘化钾 → N-butyl-3,3-bis(diethoxyphosphinyl)propionamide

https://huagongshe.com/zh-CN/reaction/1972

反应方程式

参与物

角色名称HCID投料
反应物碘化钾HCID 4875—
反应物Halite (NaCl)HCID 5234—
反应物四乙基亚甲基二磷酸脂HCID 15455—
反应物氢化钠HCID 24758—
反应物HydrideHCID 166653—
反应物N-丁基-2-氯乙酰胺HCID 219645—
溶剂四氢呋喃HCID 8028—
产物N-butyl-3,3-bis(diethoxyphosphinyl)propionamideHCID 1968904470%

反应步骤

Tetraethyl methylenebisphosphonate (1.44 g, 5.0 mmol) in THF (1 mL) was added to a slurry of 80% sodium hydride (150 mg, 5.0 mmol) in THF (4 mL) at 0° C. The reaction was warmed to room temperature and stirred until all of the hydride was consumed. A solution of N-butyl-2-chloroacetamide (0.75 g, 5.0 mmol) in THF (1 ml) and potassium iodide (100 mg) were then added. The reaction mixture was then heated at 50° C. for 18 hours, during which time sodium chloride precipitated. Additional sodium hydride (20 mg) was added, and the reaction mixture was heated an additional 4 hours. After cooling, the mixture was poured into 1N HCl (10 mL) and diethyl ether (50 mL) was added. The diethyl ether layer was further extracted with water (3×10 mL). The combined aqueous fractions were extracted with dichloromethane (4×25 mL). The combined extracts were dried (Na2SO4) and concentrated to give the title compound (1.40 g, 70%) as an oil.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US05728650
来源数据集uspto-grants-1998_03
ORD IDord-0d06fa7cb400433aac9523d5cb4e75c0
来源说明uspto-grants-1998_03