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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1645542생성일: 2026년 10월 26일

Dimethylformamide → 5-Benzyloxy-2,2-dimethyl-1,3-dioxane

https://huagongshe.com/reaction/1645542

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Benzyl BromideHCID 7498—
반응물Sodium hydrideHCID 24758—
반응물2,2-Dimethyl-1,3-dioxan-5-olHCID 11029884—
촉매Tetrabutylammonium IodideHCID 67553—
용매WaterHCID 962—
생성물5-Benzyloxy-2,2-dimethyl-1,3-dioxaneHCID 2036488954.5%

반응 단계

To a N,N-dimethylformamide (200 ml) solution of the 2,2-dimethyl-1,3-dioxan-5-ol (7.1 g, 0.054 mol) obtained in the step (9a), sodium hydride, in oil (2.81 g, 0.064 mol as the content was regarded as 55%) was added at 0° C. and stirred. After benzyl bromide (12.9 ml, 0.108 mol) and tetrabutylammonium iodide (220 mg, 0.001 mol) were added at the same temperature to the mixture, the mixture was stirred at room temperature for 1.5 hours. Water was added to the reaction mixture, which was then extracted with ethyl acetate three times. Organic layers were combined, washed five times with water and once with a saturated saline solution, dried over anhydrous sodium sulfate, and filtered. After NH silica gel was added, the resultant mixture was concentrated and purified by silica gel column chromatography (elution solvent: heptane, heptane/ethyl acetate=9/1, 4/1, ethyl acetate) to obtain the title compound (6.5 g, 54.5%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08124780B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-3ed6ca2a0d234cbb978cc9a7de249aba
출처 메모uspto-grants-2012_02