戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1368548作成日:2026年10月27日

Water → HCID 178450084、化合物

https://huagongshe.com/reaction/1368548

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
反応物1-(6-Fluoromethyloxynaphthalen-2-yl)-2-methyl-1-(1-trityl-1H-imidazol-4-yl)-1-propanol 2-Bromo-6-fluoromethyloxynaphthaleneHCID 18520208—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物HCID 178450084HCID 178450084212.7%

反応条件

温度-70 °C

反応手順

Production of 1-(6-Fluoromethyloxynaphthalen-2-yl)-2-methyl-1-(1-trityl-1H-imidazol-4-yl)-1-propanol 2-Bromo-6-fluoromethyloxynaphthalene (2.10 g) was dissolved in ether (100 ml), and the solution was cooled to −70° C. To the solution was slowly added a solution of n-butyllithium in hexane (1.6 M, 5.7 ml), and the mixture was stirred at −70° C. for 20 min. To the mixture was added dropwise a solution of 4-formyl-1-trityl-1H-imidazole (1.58 g) in THF (10 ml). The mixture was stirred for 20 min at −70° C. To the mixture was added water, and the mixture was extracted with ethyl acetate and dried. The solvent was distilled off and the residue was purified by silica gel chromatography (eluent, hexane:ethyl acetate=1:1) followed by recrystallization from diisopropyl ether to give the titled compound (1.73 g) as colorless needles.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06573289B1
出典データセットuspto-grants-2003_06
ORD IDord-3393665c27394134946795a64bd73413
出典メモuspto-grants-2003_06