戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 393312作成日:2026年10月24日

2-(Hydroxymethyl)-4-iodophenol → 5-Iodosalicylaldehyde

https://huagongshe.com/ja/reaction/393312

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Hydroxymethyl)-4-iodophenolHCID 12545259—
触媒HCID 178418406HCID 178418406—
溶媒AcetoneHCID 180—
生成物5-IodosalicylaldehydeHCID 252612—

反応手順

To a stirred solution of 2-hydroxy-5-iodobenzyl alcohol (43.5 g, 174.0 mmol) in acetone (700 mL) was added 85% activated manganese (IV) oxide (5 micron, 50 g, 494.0 mmol) and the solution stirred at room temperature for 16 hours. The manganese oxide was removed by filtration through diatomaceous earth and the filtrate concentrated in vacuo. The product was purified by flash silica chromatography (0-20% ethyl acetate in hexanes). The 2-hydroxy-5-iodobenzaldehyde was obtained as a greenish-yellow solid (24.3 g, 58%). A small amount of the 2-hydroxy-5-iodobenzaldehyde was recrystallized from methanol/water to afford an analytical sample and the remainder of the compound was used without further purification: mp 99-101° C. 1H NMR (CDCl3/300 MHz) 9.83 (s, 1H), 7.79 (d, 1H, J=2.2 Hz), 7.77 (dd, 1H, J=8.7 Hz, J=2.2 Hz), 6.81 (d, 1H, J=8.7 Hz). ESHRMS 246.9229 (M−H Calc'd 246.9256).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06806288B1
出典データセットuspto-grants-2004_10
ORD IDord-069af8e587714270ba4689d4c2b9b142
出典メモuspto-grants-2004_10