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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78207생성일: 2026년 10월 24일

Propargyl bromide → 4-[(2-Propynyloxy)methyl]benzyl alcohol

https://huagongshe.com/ko/reaction/78207

반응식

참여 물질

역할이름HCID투입량
반응물Propargyl bromideHCID 7842—
반응물TetrahydrofuranHCID 8028—
반응물1,4-BenzenedimethanolHCID 11506—
반응물Sodium hydrideHCID 24758—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-[(2-Propynyloxy)methyl]benzyl alcoholHCID 5452013158%

반응 단계

To a mixture of sodium hydride (400 mg, 8.4 mmol, 50% in oil) and tetrahydrofuran (30 mL) was added 1,4-benzenedimethanol (2.3 g, 17 mmol) at 0° C., and then N,N-dimethylformamide (30 mL) was added. The reaction mixture was stirred at room temperature for 10 minutes, after which propargyl bromide (1.0 g, 8.4 mmol) was added dropwise to the reaction mixture at 0° C. The reaction mixture was stirred at room temperature for 1 hour, after which water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was washed and saturated aqueous sodium chloride, and was concentrated under a reduced pressure. The residue thus obtained was purified by NH silica gel column chromatography (heptane:ethyl acetate=3:2) to obtain the title compound (860 mg, 58%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841327B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-97fe8d2391d4406db3bd358729a1d61d
출처 메모uspto-grants-2014_09