戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 480445作成日:2026年10月25日

Trifluoromethanesulfonic anhydride → 6-[1-Hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl]-2-naphthyl Trifluoromethanesulfonate

https://huagongshe.com/reaction/480445

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoromethanesulfonic anhydrideHCID 67749—
反応物6-(1-hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl)-2-naphtholHCID 22018385—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物6-[1-Hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl]-2-naphthyl TrifluoromethanesulfonateHCID 22285055—

反応条件

温度0 °C

反応手順

Trifluoromethanesulfonic anhydride (9.1 mL) was added dropwise to a solution of 6-(1-hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl)-2-naphthol (27.0 g) in pyridine (200 mL) at 0° C. The reaction mixture was stirred for 1 h at 0° C., diluted with water and extracted with ethyl acetate. The organic layer was washed with brine, dried and concentrated. The residue was purified by silica gel column chromatography (eluent; hexane-ethyl acetate=1:1). Crystallization from diisopropyl ether gave the titled compound (29.6 g) as a colorless powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06649643B1
出典データセットuspto-grants-2003_11
ORD IDord-572bb105840e4666833adeae9b41221f
出典メモuspto-grants-2003_11