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HRID 1691061생성일: 2026년 10월 27일

Ammonium Chloride → 4-((5-Chloro-furan-2-yl)-hydroxy-methyl)-benzonitrile

https://huagongshe.com/reaction/1691061

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참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물4-IodobenzonitrileHCID 76467—
반응물5-Chloro-2-furaldehydeHCID 2769630—
반응물HCID 178418918HCID 178418918—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-((5-Chloro-furan-2-yl)-hydroxy-methyl)-benzonitrileHCID 59255116105.4%

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온도0 °C

반응 단계

To a mixture of 4-iodobenzonitrile (3.0 g, 13 mmol) and tetrahydrofuran (40 mL) was added dropwise isopropyl magnesium chloride (1-2 M diethyl ether solution, 11 mL, 11-22 mmol) at −78° C., which was stirred for 1 hour at 0° C. The reaction mixture was cooled to −78° C., 5-chloro-2-furaldehyde (2.2 g, 17 mmol) was added at that temperature, and the temperature was gradually raised to 0° C. Following 30 minutes of stirring at 0° C., saturated aqueous ammonium chloride solution, water and ethyl acetate were added to extract the reaction mixture. The organic layer was washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. Ethyl acetate was added to the residue, which was then filtered with NH silica gel. The filtrate was concentrated under a reduced pressure to obtain the title compound (3.2 g) as a crude product. This compound was used in the subsequent reaction without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08153662B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-0490ca2bc323481e8b619c953da2965f
출처 메모uspto-grants-2012_04