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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1386643생성일: 2026년 10월 25일

1-Iodohexane → Dimethyl 2-(4-phenoxyphenyl)-2-n-hexylmalonate

https://huagongshe.com/reaction/1386643

반응식

참여 물질

역할이름HCID투입량
반응물1-IodohexaneHCID 12527—
반응물Sodium hydrideHCID 24758—
반응물Dimethyl 2-(4-phenoxyphenyl)malonateHCID 15540880—
용매TetrahydrofuranHCID 8028—
생성물Dimethyl 2-(4-phenoxyphenyl)-2-n-hexylmalonateHCID 2118303782.4%

반응 단계

To a suspension of NaH (144 mg of 60% in mineral oil washed with hexanes, 86.4 mg, 3.6 mmol) in dry THF (20 mL) was carefully added dimethyl 2-(4-phenoxyphenyl)malonate (900 mg, 3.0 mmol). The resulting mixture was stirred at room temperature for 1 hour and then 1-iodohexane (1.27 g, 0.89 mL, 6.0 mmol) was added. The reaction mixture was stirred at room temperature for 1 hour and then heated to reflux overnight . The reaction was cooled to room temperature and quenched with 1N HCl (20 mL) and extracted with ether (2×40 mL). The combined organic extracts were washed with saturated Na2S2O3, water, then brine, dried (Na2SO4), concentrated, and purified by chromatography using a Chromatotron with a silica gel plate (4000 micron) eluted with 13% EtOAc/hexanes to give 950 mg of dimethyl 2-(4-phenoxyphenyl)-2-n-hexylmalonate as a viscous oil. 1H NMR (200 mHz, CDCl3) δ 7.39-6.92 (9H, m), 3.75 (6H, s), 2.10 (2H, t), 1.29 (8H, m), 0.87 (3H, t).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06265578B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-51c84c1908ed4bb0a55197e469e605b4
출처 메모uspto-grants-2001_07