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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 548756생성일: 2026년 10월 26일

Water → 2-[3-(2,4-Difluorophenyl)sulfanylpropoxy]oxane

https://huagongshe.com/reaction/548756

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물2,4-Difluorobenzene-1-thiolHCID 2737073—
반응물2-(3-Bromopropoxy)tetrahydro-2H-pyranHCID 2777988—
용매TetrahydrofuranHCID 8028—
생성물2-[3-(2,4-Difluorophenyl)sulfanylpropoxy]oxaneHCID 5766322577.2%

반응 단계

Sodium hydride (60% dispersion in mineral oil) (120 mg, 3.01 mmol) was added to a solution of 2,4-difluorothiophenol (0.4 g, 2.74 mmol) in THF (10 mL) at 0° C., under argon. The reaction was allowed to warm to RT and 2-(3-bromopropoxy)tetrahydro-2H-pyran (672 mg, 3.01 mmol) added. The reaction was stirred at RT for 4 hours then poured into iced water (50 mL) and extracted into ethyl acetate (50 mL). The organics were washed with brine (50 mL), dried (MgSO4), filtered and the solvent removed in vacuo to give a yellow oil which was chromatographed on silica, eluting with 0-10% ethyl acetate in isohexane, to give the desired compound as a colourless oil (610 mg). 1H NMR δ (CDCl3): 1.49-1.61 (m, 4H), 1.65-1.73 (m, 1H), 1.75-1.90 (m, 3H), 2.96 (t, 2H), 3.46-3.52 (m, 2H), 3.79-3.87 (m, 2H), 4.55-4.56 (m, 1H), 6.80-6.86 (m, 2H), 7.38-7.44 (m, 1H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07943607B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-625c799b1a68490c8e253edfa9f45702
출처 메모uspto-grants-2011_05