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HRID 71244作成日:2026年10月23日

Allyl acetate → 2-Allyl-2-phenylcyclohexanone

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

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl acetateHCID 11584—
反応物2-PhenylcyclohexanoneHCID 95592—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
触媒TriphenylphosphineHCID 11776—
触媒Palladium, di-mu-chlorobis(eta3-2-propenyl)di-HCID 61538—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2-Allyl-2-phenylcyclohexanoneHCID 1302321491%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822510B2
出典データセットuspto-grants-2014_09
ORD IDord-4bf53f38610e470695b5ca8f34b66570
出典メモuspto-grants-2014_09