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HRID 1970생성일: 2026년 10월 23일

Tetrahydrofuran → Tetraethyl 3-oxopentane-1,1-bisphosphonate

https://huagongshe.com/ko/reaction/1970

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물HydrideHCID 166653—
반응물N-methoxy-N-methyl-3,3-bis(diethoxyphosphinyl)propionamideHCID 19689023—
생성물Tetraethyl 3-oxopentane-1,1-bisphosphonateHCID 1249940754%

반응 조건

온도-78 °C

반응 단계

A solution of N-methoxy-N-methyl-3,3-bis(diethoxyphosphinyl)propionamide (1.00 g, 2.6 mmol) in THF (5 ml) was slowly added to a slurry of 80% sodium hydride (80 mg, 2.7 mmol) in THF (10 ml) at 0° C. Stirring was continued until all of the hydride was consumed (~20 minutes). The solution was cooled to -78° C. and ethylmagnesium bromide (1.0 ml of a 3.0M solution in diethyl ether, 3.0 mmol) was added. After the addition, the reaction mixture was warmed to 0° C. and stirred for one hour. The reaction was quenched by pouring slowly into a well-stirred ice-cold mixture of ethanol (40 ml) and concentrated HCl (5 ml). The solvents were removed in vacuo, the residue was taken up in brine (20 ml) and extracted with dichloromethane (4×20 ml). The combined extracts were dried (Na2SO4), concentrated in vacuo, and the resulting oil was purified by flash chromatography on silica gel eluting with 10% i-propanol in ethyl acetate to give the title compound (0.50 g, 54%) as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728650
출처 데이터셋uspto-grants-1998_03
ORD IDord-513ee407692540e49f626f2d20b712d3
출처 메모uspto-grants-1998_03