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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 466267생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/466267

반응식

참여 물질

역할이름HCID투입량
반응물Potassium periodateHCID 516896—
반응물{[(2-Methylpent-4-EN-1-YL)oxy]methyl}benzeneHCID 14608667—
촉매Osmium TetroxideHCID 30318—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물(R)-4-Benzyloxy-3-methylbutanalHCID 1111687581%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05155228
출처 데이터셋uspto-grants-1992_10
ORD IDord-32bef3fdc944401e9dfafddf455ae440
출처 메모uspto-grants-1992_10