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HRID 562596作成日:2026年10月27日

2-Methyl-4-nitrophenol → 2-Methyl-1-(2-methyl-4-nitrophenoxy)propan-2-ol

https://huagongshe.com/reaction/562596

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-4-nitrophenolHCID 7442—
反応物Isobutylene oxideHCID 11208—
反応物Potassium CarbonateHCID 11430—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
溶媒Sodium BicarbonateHCID 516892—
生成物2-Methyl-1-(2-methyl-4-nitrophenoxy)propan-2-olHCID 5754060690.3%

反応手順

A mixture of 2-methyl-4-nitrophenol (5.50 g, 35.9 mmol), 2,2-dimethyloxirane (7.77 g, 108 mmol), K2CO3 (4.96 g, 35.9 mmol) and NaH2PO4 (4.31 g, 35.9 mmol) in MeCN (50 mL) and H2O (8.82 mL) was stirred at 140° C. in a steel bomb for 6 hours. After cooling to RT, the reaction was diluted with aq. saturated NaHCO3 (80 ml) prior to extraction with EtOAc (100 ml). The EtOAc layer was dried over Na2SO4 and concentrated. The crude product was purified by silica gel chromatography employing a solvent gradient (hexane to 60% ethyl acetate) to elute 2-methyl-1-(2-methyl-4-nitrophenoxy)propan-2-ol (7.3 g, 32.4 mmol, 90% yield) as yellow oil. MS (M+1=226). 1H NMR (500 MHz, chloroform-d) δ ppm 8.00-8.15 (2H, m), 6.86 (1H, d, J=8.80 Hz), 3.90 (2H, s), 2.33 (3H, s), 1.40 (6H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067420B2
出典データセットuspto-grants-2011_11
ORD IDord-4c1de9f843dd41b79fa4927fad584c96
出典メモuspto-grants-2011_11