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HRID 261925생성일: 2026년 10월 25일

CID 406 → Dimethyl 2-Oxo-3-(2-norbornyl)propylphosphonate

https://huagongshe.com/reaction/261925

반응식

참여 물질

역할이름HCID투입량
반응물CID 406HCID 406—
반응물Dimethyl methylphosphonateHCID 12958—
반응물Methyl 2-{bicyclo[2.2.1]heptan-2-yl}acetateHCID 13403348—
반응물ButyllithiumHCID 178418339—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Dimethyl 2-Oxo-3-(2-norbornyl)propylphosphonateHCID 21321713—

반응 단계

A solution of 63.9 g (0.516 mole) dimethyl methylphosphonate (Aldrich) in 645 ml dry tetrahydrofuran was cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution was added 251 ml of 2.2 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 40 minutes at such a rate that the reaction temperature never rose about -65°. After an additional 5 minutes stirring at -78°, 43.5 g (0.258 mole) methyl (2-norbornyl)acetate 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 35 ml acetic acid and rotary evaporated to a white gel. The gelatinous material was taken up in 50 ml water, the aqueous phase extracted with 100 ml portions of chloroform (4x), the combined organic extracts were backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, dimethyl 2-oxo-3-(2-norbornyl) propylphosphonate (b.p. 138°-141°/0.3 mm).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04152527
출처 데이터셋uspto-grants-1979_05
ORD IDord-e46a6230018340348bda05f58aa5ab2c
출처 메모uspto-grants-1979_05