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HRID 1278025생성일: 2026년 10월 27일

Solketal → 5-[[(2,2-Dimethyl-1,3-dioxolan-4-yl)-methoxy]methyl]tetrahydro-2-furanmethanol

https://huagongshe.com/reaction/1278025

반응식

참여 물질

역할이름HCID투입량
반응물SolketalHCID 7528—
반응물1,2:5,6-DiepoxyhexaneHCID 15903—
반응물Sodium hydrideHCID 24758—
용매WaterHCID 962—
생성물5-[[(2,2-Dimethyl-1,3-dioxolan-4-yl)-methoxy]methyl]tetrahydro-2-furanmethanolHCID 1288874858.1%

반응 단계

46.3 g of 2,2-dimethyl-1,3-dioxolane-4-methanol (0.35 mol) (Aldrich) is cooled to 0° in an ice bath and under a nitrogen atmosphere 2.1 g of sodium hydride (0.088 mol) (washed with hexane to remove the mineral oil) is slowly added to the rapidly stirred mixture. The addition of the sodium hydride is made at such a rate that the temperature remains below 20°. After the addition of the NaH has been completed the mixture is allowed to stir for 1/2 hour and slowly warmed to room temperature. Slowly, and with stirring 10.0 g of 1,5-hexadiene diepoxide (0.088 mol) is added to the mixture. After the addition of the diepoxide has been completed the reaction mixture is heated at reflux for 16 hours. The mixture is then cooled to room temperature and with stirring is poured into 350 ml of water. The aqueous mixture is extracted with two 200 ml portions of chloroform, the CHCl3 extracts are combined and dried over anhydrous sodium sulfate. The CHCl3 is removed in vacuo and the dark brown residue then vacuum distilled through a 10 cm vigreux distilling column. The fraction boiling at 135°-137° @ 0.3 mm is collected yielding 12.6 g (58%) of the above compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04279902
출처 데이터셋uspto-grants-1981_07
ORD IDord-6d4df769bad748f798d2d078e499b120
출처 메모uspto-grants-1981_07