戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 575463作成日:2026年10月24日

Potassium Carbonate → (1-((4-Iodo-2-nitrophenoxy)methyl)cyclopropyl)methanol

https://huagongshe.com/ja/reaction/575463

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1,1-Bis(hydroxymethyl)cyclopropaneHCID 4101437—
反応物1-Fluoro-4-iodo-2-nitrobenzeneHCID 14590582—
溶媒DimethylformamideHCID 6228—
生成物(1-((4-Iodo-2-nitrophenoxy)methyl)cyclopropyl)methanolHCID 8669352771%

反応条件

温度50 °C

反応手順

A solution of 1-fluoro-4-iodo-2-nitrobenzene (2.50 g, 9.4 mmol) in DMF (30 mL) was treated with 1-(hydroxymethyl)cyclopropylmethanol (1.91 g, 19 mmol) and K2CO3 (2.6 g, 19 mmol) and the mixture was heated at 50° C. for 8 hours. TLC indicated complete consumption of the arylfluoride. The mixture was diluted with water and extracted with ethyl acetate. The combined organics were washed with brine, dried over sodium sulfate and concentrated by rotoevaporation. Purification by flash column chromatography (EtOAc in heptanes) gave the titled compound as a light yellow solid (2.31 g, 71% yield). 1H NMR (400 MHz, DMSO) δ 8.15 (d, J=2.2 Hz, 1H), 7.92 (dd, J=8.8, 2.2 Hz, 1H), 7.17 (d, J=8.9 Hz, 1H), 4.60 (t, J=5.6 Hz, 1H), 4.05 (s, 2H), 3.36 (d, J=5.6 Hz, 2H), 0.50 (s, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09034866B2
出典データセットuspto-grants-2015_05
ORD IDord-af1aafb3e9064f4bac3bdba56441a578
出典メモuspto-grants-2015_05