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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1606579생성일: 2026년 10월 26일

CID 406 → Dimethyl 2-oxo-undecylphosphonate

https://huagongshe.com/reaction/1606579

반응식

참여 물질

역할이름HCID투입량
반응물CID 406HCID 406—
반응물Methyl DecanoateHCID 8050—
반응물Dimethyl methylphosphonateHCID 12958—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Dimethyl 2-oxo-undecylphosphonateHCID 10612624—

반응 단계

A solution of 49.6 g. (0.40 mole) dimethyl methylphosphonate (Aldrich) in 500 ml. dry tetrahydrofuran is cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution is added 188 ml. of 2.34 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 above -65°. After an additional 5 minutes stirring at -78°, 36.3 g. (0.20 mole) methyl decanoate is added dropwise at a rate that kept the reaction temperature less than -70° (20 minutes). After 1.0 hour at -78° the reaction mixture is allowed to warm to ambient temperature, neutralized with 25 ml. acetic acid and rotary evaporated to a white gel. The gelatinous material is taken up in 75 ml. water, the aqueous phase extracted with 100 ml. portions of chloroform (3x), the combined organic extracts are backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, to give dimethyl 2-oxo-undecylphosphonate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03953466
출처 데이터셋uspto-grants-1976_04
ORD IDord-dd1dd85ce54b4e2e8e59589fd180eae7
출처 메모uspto-grants-1976_04