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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 322606생성일: 2026년 10월 27일

Acetone → 3,5-Di(3,5-di(4-vinylbenzyloxy)benzyloxy)benzylalcohol

https://huagongshe.com/reaction/322606

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Potassium CarbonateHCID 11430—
반응물3,5-Dihydroxybenzyl alcoholHCID 34661—
반응물3,5-Bis(4-vinylbenzyloxy)benzyl bromideHCID 18433945—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물3,5-Di(3,5-di(4-vinylbenzyloxy)benzyloxy)benzylalcoholHCID 1843394481.9%

반응 단계

A 250 ml flask is charged with 15 g (34.5 mmol, 2.2 eq) of bromide (2) and acetone (100 ml) under an argon atmosphere. To this solution is added 3,5-dihydroxybenzyl alcohol (2.2 g, 15.7 mmol), 0.82 g (31. mmol, 0.2 eq) 18-C-6 and 4.77 g (34-5 mmol, 2.2 eq) of K2CO3 and the mixture is stirred for 48 hours whereupon a yellow suspension is formed. To the mixture is added methylene chloride (200 ml) and water (200 ml). The organic phase is separated, dried over MgSO4 and evaporated to dryness. A dark brown oil is obtained which is dissolved in toluene (40 ml) and hexane (20 ml). Upon cooling, a white powder forms which is collected by filtration to give 10.92 g (81.9% of (3A).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211316B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-7c38a8d86c804a088e9b4407bbaf07ed
출처 메모uspto-grants-2001_04