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HRID 261923생성일: 2026년 10월 27일

CID 406 → Dimethyl (3-cyclohexyl-2-oxopropyl)phosphonate

https://huagongshe.com/reaction/261923

반응식

참여 물질

역할이름HCID투입량
반응물CID 406HCID 406—
반응물Dimethyl methylphosphonateHCID 12958—
반응물Cyclohexaneacetic acid, methyl esterHCID 139743—
반응물ButyllithiumHCID 178418339—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Dimethyl (3-cyclohexyl-2-oxopropyl)phosphonateHCID 14302183—

반응 단계

A solution of 49.6 g (0.40 mole) dimethyl methylphosphonate (Aldrich) in 500 ml dry tetrahydrofuran was cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution was 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°, 31.2 g (0.20 mole) methylcyclohexylacetate 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 25 ml acetic acid and rotary evaporated to a white gel. The gelatenous material was taken up in 75 ml water, the aqueous phase extracted with 100 ml portions of chloroform (3x), the combined organic extracts were backwashed (50 cc H 2 O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, b.p. 160°-162° (0.2 mm) to give dimethyl 2-oxo-3-cyclohexylpropylphosphonate (2h).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04152527
출처 데이터셋uspto-grants-1979_05
ORD IDord-d805ae2a3b1d4b668f257981756fa8e8
출처 메모uspto-grants-1979_05