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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132099생성일: 2026년 10월 26일

3-Oxo-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester → 3-Methylene-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester

https://huagongshe.com/reaction/132099

반응식

참여 물질

역할이름HCID투입량
반응물3-Oxo-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl esterHCID 59733780—
반응물ButyllithiumHCID 178418339—
촉매Methyltriphenyliphosphonium bromideHCID 74505—
용매TetrahydrofuranHCID 8028—
생성물AcetateHCID 175—
생성물3-Methylene-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl esterHCID 59733752100%

반응 조건

온도-10 °C

반응 단계

A solution of 1.6 M n-butyllithium in hexanes (14.0 mL, 22.4 mmol) was added to a heterogeneous mixture of methyltriphenylphosphonium bromide (8.02 g, 22.4 mmol) in tetrahydrofuran (50 mL) at −10° C. After stirring for 30 min at −10° C., the yellow slurry was cooled to −78° C. and 3-oxo-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester (3.41 mg, 14.1 mmol) in tetrahydrofuran (20 mL) was added. After stirring for 10 min at −78° C., the dry ice/acetone bath was removed and the heterogeneous mixture was stirred for 3 h, during which time the solution warmed to ambient temperature. The heterogeneous mixture was concentrated and the residue was flash chromatographed with 99:1, 49:1, 24:1, and 23:2 hexanes:etheyl acetate as the eluant to yield 3.38 g (100% yield) of 3-methylene-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07385085B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-2574301570b546bbbd04d4f66b8d5256
출처 메모uspto-grants-2008_06