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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-4-nitrophenol | HCID 7442 | — |
| Reactant | Isobutylene oxide | HCID 11208 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 2-Methyl-1-(2-methyl-4-nitrophenoxy)propan-2-ol | HCID 57540606 | 90.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067420B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-4c1de9f843dd41b79fa4927fad584c96 |
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| Source note | uspto-grants-2011_11 |
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