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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71244생성일: 2026년 10월 24일

Allyl acetate → 2-Allyl-2-phenylcyclohexanone

https://huagongshe.com/ko/reaction/71244

반응식

참여 물질

역할이름HCID투입량
반응물Allyl acetateHCID 11584—
반응물2-PhenylcyclohexanoneHCID 95592—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
촉매TriphenylphosphineHCID 11776—
촉매Palladium, di-mu-chlorobis(eta3-2-propenyl)di-HCID 61538—
용매1,2-DimethoxyethaneHCID 8071—
생성물2-Allyl-2-phenylcyclohexanoneHCID 1302321491%

반응 단계

To a solution of 2-phenylcyclohexanone (2 g, 11.48 mmol) in 50 ml of anhydrous DME in an ice bath was added 1M sodium bis(trimethylsilyl)amide (12.63 mL, 12.63 mmol) dropwise and the solution was stirred at the same temp for 20 minutes. In a separated flask allylpalladium chloride dimer (0.104 g, 0.287 mmol) was dissolved in 10 ml of anhydrous DME, and was added triphenylphosphine (0.151 g, 0.574 mmol) to the solution. It was stirred for 20 minutes at room temp and then allyl acetate (1.300 mL, 12.05 mmol) was added. This solution was added to the anion solution dropwise and the mixture was stirred at room temp for 2 hrs. The reaction was quenched with saturated NH4Cl and extracted with hexane. The organic layer was washed with brine. The combine aqueous layers were back-extracted with hexane once and combined. Dried over Na2SO4 and evaporated to give an oily residue. It was purified by Combiflash (120 g silica gel) eluting with hexane followed by 1:9 EtOAc-hexane to give 2.24 g of 2-allyl-2-phenylcyclohexanone. 1H NMR (400 MHz, CCl3D) δ ppm 7.35 (2H, t, J=7.58 Hz), 7.21-7.27 (1H, m), 7.12-7.18 (2H, m), 5.35-5.52 (1H, m), 4.82-4.97 (2H, m), 2.61-2.72 (1H, m), 2.39-2.55 (2H, m), 2.24-2.38 (2H, m), 1.89-1.99 (1H, m, J=9.39, 6.15, 2.88, 2.88 Hz), 1.62-1.81 (4H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822510B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4bf53f38610e470695b5ca8f34b66570
출처 메모uspto-grants-2014_09