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HRID 389442作成日:2026年10月26日

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

https://huagongshe.com/reaction/389442

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 5954116594.1%

反応条件

温度60 °C

反応手順

A mixture of 1-(1,4-dioxa-spiro[4.5]dec-8-yl)-4-iodo-1H-pyrazole (338 mg, 1.00 mmol), pyridinium p-toluenesulfonate (518 mg, 2.00 mmol), acetone (15 mL) and H2O (15 mL) was heated at 60° C. for 2 d. The mixture was extracted with EtOAc (3×30 mL). The combined extracts were washed with water (3×30 mL), brine (30 mL), dried over MgSO4, and concentrated in vacuo leaving 273 mg (89%) of the title compound as a white solid. 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 (ESI): 291.09 [M+H]+; HPLC tR=2.80 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08378104B2
出典データセットuspto-grants-2013_02
ORD IDord-dadb140749e848dcafc4fa6e18ef3b03
出典メモuspto-grants-2013_02