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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562596Generated: October 25, 2026

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

https://huagongshe.com/reaction/562596

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-4-nitrophenolHCID 7442—
ReactantIsobutylene oxideHCID 11208—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
Product2-Methyl-1-(2-methyl-4-nitrophenoxy)propan-2-olHCID 5754060690.3%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067420B2
Source datasetuspto-grants-2011_11
ORD IDord-4c1de9f843dd41b79fa4927fad584c96
Source noteuspto-grants-2011_11