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HRID 261922생성일: 2026년 10월 27일

CID 406 → Dimethyl 2-Oxo-4-(1-Adamantyl)butylphosphonate

https://huagongshe.com/reaction/261922

반응식

참여 물질

역할이름HCID투입량
반응물CID 406HCID 406—
반응물Dimethyl methylphosphonateHCID 12958—
반응물Methyl 3-(1-adamantyl)propanoateHCID 10889502—
반응물ButyllithiumHCID 178418339—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Dimethyl 2-Oxo-4-(1-Adamantyl)butylphosphonateHCID 21321716100%

반응 단계

A solution of 24.8 g (0.200 moles) dimethyl methyl-phosphonate (Aldrich) in 250 ml dry tetrahydrofuran was cooled to -78° in a dry nitrogen atomsphere. To the stirred phosphonate solution was added 92 ml of 2.38 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 30 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 22.2 g (0.100 mole) methyl 3-(1-adamantyl)propionate was added dropwise at a rate that kept the reaction temperature less than -70° (20 minutes). After 1.0 hour at -78° the reaction mixture was allowed to warm to ambient temperature, neutralized with 55 ml acetic acid and rotary evaporated to a white gel. The gelatenous material was taken up to 50 ml water, the aqueous phase extracted with 100 ml portions of methylene chloride (4X), the combined organic extracts were backwashed with water (4 × 100 ml), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, b.p. 195-200° (<0.02 mm) to give dimethyl 2-oxo-4-(1-adamantyl)butylphosphonate (2b) weighing 36.6 g (100% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04152527
출처 데이터셋uspto-grants-1979_05
ORD IDord-d74267ae4f9840bd8c5b44a792da3ddb
출처 메모uspto-grants-1979_05