돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51306생성일: 2026년 10월 25일

Chlorotrimethylsilane → Ethyl 3-cyclohexyl-3-methylbutanoate

https://huagongshe.com/reaction/51306

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물Ethyl 3,3-dimethylacrylateHCID 12516—
반응물Ammonium ChlorideHCID 25517—
반응물HCID 178478990HCID 178478990—
촉매Cuprous chlorideHCID 62652—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 3-cyclohexyl-3-methylbutanoateHCID 22289815—

반응 단계

Trimethylsilyl chloride (1.3 ml, 10.2 mmol), copper (I) chloride (30 mg, 0.3 mmol) and cyclohexylmagnesium chloride (4.6 ml, 2N in diethyl ether, 9.2 mmol) were added slowly to an ice-cooled solution of ethyl 3,3-dimethylacrylate (1 g, 8.5 mmol) in tetrahydrofuran (10 ml). The solution was stirred for 10 minutes, then allowed to warm to room temperature and stirred for an hour. Saturated aqueous ammonium chloride solution (10 ml) was added and the mixture was partitioned between water (10 ml) and diethyl ether (20 ml). The layers were separated and the aqueous phase was extracted with diethyl ether (2×10 ml). The combined organic extracts were dried (MgSO4) and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel using ethyl acetate:pentane(5:95) as eluant to afford the title compound, 1.2 g. 1H-NMR (CDCl3, 400 MHz) δ: 0.75 (m, 8H), 1.05-1.28 (m, 7H), 1.62 (m, 1H), 1.78 (m, 4H), 2.20 (s, 2H), 4.10 (q, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713496B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-34c3090648704563a602edad49707405
출처 메모uspto-grants-2004_03