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HRID 511338作成日:2026年10月25日

Acetone → 4-(4-iodo-1H-pyrazol-1-yl)cyclohexanone

https://huagongshe.com/reaction/511338

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
反応物1-(1,4-Dioxaspiro[4.5]dec-8-yl)-4-iodo-1H-pyrazoleHCID 59541125—
溶媒WaterHCID 962—
生成物4-(4-iodo-1H-pyrazol-1-yl)cyclohexanoneHCID 59541165—

反応条件

温度60 °C

反応手順

A mixture of 1-(1,4-dioxaspiro[4.5]dec-8-yl)-4-iodo-1H-pyrazole (Compound 137F, 3.0 g, 8.9 mmol), pyridinium p-toluenesulfonate (4.5 g, 17.9 mmol), acetone (100 mL) and H2O (100 mL) was heated at 60° C. overnight. Work-up: Solvent was evaporated and the residue was extracted with EtOAc (3×60 mL). The combined extracts were washed with water (3×50 mL), brine (50 mL), dried over Na2SO4, filtered, and concentrated in vacuo to give the title compound as white solid. It was used in the next step without further purification. 1H NMR (400 MHz, CDCl3): δ=2.23-2.63 (m, 8 H), 4.57-4.64 (m, 1 H), 7.51 (s, 1 H), 7.54 (s, 1 H). MS (ES+): m/z=291.09 (100). HPLC: tR=2.79 min (polar—5 min, ZQ3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096624B2
出典データセットuspto-grants-2015_08
ORD IDord-80f03c31f257450fb7fdd2f7858debbb
出典メモuspto-grants-2015_08