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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 562596생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/562596

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-4-nitrophenolHCID 7442—
반응물Isobutylene oxideHCID 11208—
반응물Potassium CarbonateHCID 11430—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매Sodium BicarbonateHCID 516892—
생성물2-Methyl-1-(2-methyl-4-nitrophenoxy)propan-2-olHCID 5754060690.3%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08067420B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-4c1de9f843dd41b79fa4927fad584c96
출처 메모uspto-grants-2011_11