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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31565생성일: 2026년 10월 25일

Neopentyl glycol → 2-((Benzyloxy)methyl)-5,5-dimethyl-1,3-dioxane

https://huagongshe.com/reaction/31565

반응식

참여 물질

역할이름HCID투입량
반응물Neopentyl glycolHCID 31344—
반응물(Phenylmethoxy)acetaldehydeHCID 108989—
촉매p-Toluenesulfonic acid monohydrateHCID 521998—
용매TolueneHCID 1140—
생성물2-((Benzyloxy)methyl)-5,5-dimethyl-1,3-dioxaneHCID 5979255796.6%

반응 단계

To a mixture of benzyloxyacetaldehyde (5 g, 33.3 mmol), 2,2-dimethyl-1,3-propanediol (4.16 g, 40 mmol) and toluene (70 ml), p-toluenesulfonic acid monohydrate (287 mg, 1.51 mmol) was added and refluxed for 4 hours while removing water by the Dean-Stark apparatus. After the reaction mixture was cooled to room temperature, triethylamine (4 ml) was added to the reaction mixture and the solvent was removed by evaporation. The residue was purified by silica gel column chromatography (silica gel: 200 g, elution solvent: ethyl acetate/heptane=1/9) to obtain the title compound (7.6 g, yield: 96.6%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425634B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-95876f928d594ffb87130057875b8aae
출처 메모uspto-grants-2008_09