戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 7186作成日:2026年10月24日

Dimethyl Sulfoxide → 4-(Pyridin-2-ylaminomethyl)-benzaldehyde

https://huagongshe.com/ja/reaction/7186

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物(4-((Pyridin-2-ylamino)methyl)phenyl)methanolHCID 22018543—
溶媒DichloromethaneHCID 6344—
生成物4-(Pyridin-2-ylaminomethyl)-benzaldehydeHCID 2201877531%

反応条件

温度-78 °C

反応手順

To a solution of oxalyl chloride (0.9 ml, 10.32 mmol) in CH2Cl2 (15 ml) at −78° C. was added a solution of DMSO (1.5 ml, 21.11 mmol) in CH2Cl2 (10 ml) and the mixture allowed to stir for 20 min. at −78° C., after which [4-(Pyridin-2-ylaminomethyl)-phenyl]-methanol (1.1 g, 5.13 mmol) in CH2Cl2 (10 ml) was added dropwise. Stirring was continued for 2 hours and then Et3N (2.9 ml, 21.30 mmol) was added dropwise. The cooling bath was removed, stirring was continued for 3 h, and the mixture was diluted with 300 mL ethyl acetate, washed with sat. NaHCO3, brine and dried over Na2SO4. Evaporation of the solvent and purification of the residue by flash chromatography on silica gel, using 30% ethyl acetate in CH2Cl2, gave the title compound (335 mg, 31%) as a pure white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084155B2
出典データセットuspto-grants-2006_08
ORD IDord-f466dc70f6664a43a2e59685051e375f
出典メモuspto-grants-2006_08