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HRID 384323作成日:2026年10月27日

2-Bromo-4-methylphenol → 2-Bromo-4-methyl-6-nitrophenol

https://huagongshe.com/reaction/384323

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-4-methylphenolHCID 23109—
反応物Sodium NitrateHCID 24268—
溶媒WaterHCID 962—
溶媒Sulfuric AcidHCID 1118—
生成物2-Bromo-4-methyl-6-nitrophenolHCID 2991829,045.199%

反応手順

Sodium nitrate (28 g, 0.33 mmol) was dissolved in the solvent mixture of 70 mL of concentrated sulfuric acid and 210 mL of water at −5° C., followed by slowly dropwise addition of 2-bromo-4-methyl-phenol 11a (30.8 g, 0.165 mol). The reaction mixture was reacted for 2 hours upon cooling by an ice-water bath. The mixture was warmed up to room temperature and reacted for another 1 hour. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was extracted with 200 mL of ethyl acetate. The combined organic extracts were washed with water (100 mL×5), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound 2-bromo-4-methyl-6-nitro-phenol 11b (22.24 g, yield 58.1%) as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367710B2
出典データセットuspto-grants-2013_02
ORD IDord-ae8cdedc8c054f82beef374db0c36f0c
出典メモuspto-grants-2013_02