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HRID 1193025생성일: 2026년 10월 26일

Furfural → ([4-Bromo-2,6-dimethylphenyl]furan-2-yl)methanol

https://huagongshe.com/reaction/1193025

반응식

참여 물질

역할이름HCID투입량
반응물FurfuralHCID 7362—
반응물Ammonium ChlorideHCID 25517—
반응물5-Bromo-2-iodo-1,3-dimethylbenzeneHCID 2735573—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물([4-Bromo-2,6-dimethylphenyl]furan-2-yl)methanolHCID 6670961182.5%

반응 조건

온도-78 °C

반응 단계

4-Bromo-2,6-dimethyl-1-iodobenzene (5 g, 16 mmol) is dissolved in dry tetrahydrofuran (20 ml) and cooled to −78° C. under an atmosphere of dry nitrogen. Isopropylmagnesium chloride (2M solution in tetrahydrofuran, 10 ml, 20 mmol) is added dropwise with vigorous stirring over 30 minutes. When the addition is complete, the reaction is allowed to warm to room temperature and is stirred for 30 minutes at room temperature. The reaction mixture is cooled to −78° C. and a solution of 2-furaldehyde (2.4 g, 25 mmol) in dry tetrahydrofuran (10 ml) is added dropwise over 30 minutes. Once the addition is complete, the mixture is allowed to warm to room temperature and stirring continued for 2 hours. A solution of saturated aqueous ammonium chloride (30 ml). is added, and the mixture is extracted with dichloromethane (3×25 ml). The organic extracts are combined, washed with brine, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give ([4-bromo-2,6-dimethylphenyl]furan-2-yl)methanol (3.71 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08680339B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-0be7fb479df94a41b7e743df13130fc0
출처 메모uspto-grants-2014_03