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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1672692생성일: 2026년 10월 26일

Water → 1-Allyl 7-ethyl 2-allyloxycarbonyl-2-(4-cyanobenzyl)heptanedioate

https://huagongshe.com/reaction/1672692

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물4-(Bromomethyl)benzonitrileHCID 86996—
반응물1-Allyl 7-ethyl 2-allyloxycarbonylheptanedioateHCID 57831364—
용매DimethylformamideHCID 6228—
생성물1-Allyl 7-ethyl 2-allyloxycarbonyl-2-(4-cyanobenzyl)heptanedioateHCID 5783134573.4%

반응 조건

온도0 °C

반응 단계

1.69 g (70.43 mmol) of sodium hydride are added in portions to a solution of 20 g (64.03 mmol) of 1-allyl 7-ethyl 2-allyloxycarbonylheptanedioate from Example 82A in 140 ml of dimethylformamide at 0° C. The reaction mixture is then allowed to reach room temperature and is stirred for 30 min. The reaction solution is cooled to 0° C. again and, after addition of 16.32 g (83.24 mmol) of 4-bromomethylbenzonitrile in 140 ml of DMF, stirred at this temperature for 30 min. The mixture is then stirred at room temperature overnight. Water is added dropwise to the reaction mixture and, after extraction three times with ethyl acetate, the combined organic phases are washed with saturated sodium chloride solution and dried over sodium sulfate. After filtration, the solvent is concentrated to dryness in vacuo. The resulting crude product is purified by flash chromatography an silica gel (mobile phase: cyclohexane/ethyl acetate 10:1→4:1→1:1). 20.08 g (46.97 mmol, 73% yield) of a colorless solid are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07998988B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-e3d7560f89ea4c80a678b6317bff781f
출처 메모uspto-grants-2011_08