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HRID 1193025作成日:2026年10月27日

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

https://huagongshe.com/reaction/1193025

反応式

関与物質

役割名称HCID仕込み量
反応物FurfuralHCID 7362—
反応物Ammonium ChlorideHCID 25517—
反応物5-Bromo-2-iodo-1,3-dimethylbenzeneHCID 2735573—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物([4-Bromo-2,6-dimethylphenyl]furan-2-yl)methanolHCID 6670961182.5%

反応条件

温度-78 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08680339B2
出典データセットuspto-grants-2014_03
ORD IDord-0be7fb479df94a41b7e743df13130fc0
出典メモuspto-grants-2014_03