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HRID 466267作成日:2026年10月23日

Potassium periodate → (R)-4-Benzyloxy-3-methylbutanal

https://huagongshe.com/ja/reaction/466267

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium periodateHCID 516896—
反応物{[(2-Methylpent-4-EN-1-YL)oxy]methyl}benzeneHCID 14608667—
触媒Osmium TetroxideHCID 30318—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物(R)-4-Benzyloxy-3-methylbutanalHCID 1111687581%

反応手順

A 250 mL round-bottomed flask, equipped with a magnetic stirring bar and a thermometer was fitted with a septum and a nitrogen inlet. The apparatus was charged with benzyl 2-methyl-4-penten-1-yl ether (2.39 g, 12.5 mmol) in 75 mL of acetone and 25 mL of water. Osmium tetroxide (0.833 mL of an 0.15M aqueous solution, 0.125 mmol) was added in one portion, followed by potassium periodate (6.04 g, 26.2 mmol) in three equal portions. The resulting slurry was stirred for 6 hours at room temperature and decanted into a 500 mL separatory funnel. The aqueous layer was extracted with 3×200 mL of diethyl ether. Each washing was stirred over the solids for 5 minutes, washed with 150 mL of saturated aqueous sodium thiosulfate and 100 mL of saturated aqueous sodium chloride. The combined organic layers were dried over sodium sulfate, filtered, concentrated and chromatographed (4×20 cm column; 4:1 hexane:ethyl acetate) to afford 1.94 g (81%) of aldehyde 4 as a colorless oil. Rf =0.37 (4:1 hexane:ethyl acetate).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05155228
出典データセットuspto-grants-1992_10
ORD IDord-32bef3fdc944401e9dfafddf455ae440
出典メモuspto-grants-1992_10