HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 4-Bromo-2-methyl-5-nitrophenyl methyl carbonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 4-Bromo-2-methylphenyl methyl carbonate | HCID 59394985 | — |
| Product | 4-Bromo-2-methyl-5-nitrophenyl methyl carbonate | HCID 59395055 | 71.8% |
Reaction Steps
4-Bromo-2-methylphenyl methyl carbonate (4.0 g, 16.32 mmol) was added portion-wise to H2SO4 (12.0 mL) to generate a homogeneous solution. This solution was then cooled to 0° C. internal temperature and KNO3 (2.0 g, 19.6 mmol) was added portion-wise maintaining the internal temperature below 5° C. The reaction was stirred for 2 h and then poured over ice. The aqueous layer was extracted with dichloromethane, washed with saturated NaHCO3 and water, dried over Na2SO4, and concentrated. Purification by silica gel chromatography (0-5% ethyl acetate/hexanes) provided 4-bromo-2-methyl-5-nitrophenyl methyl carbonate (3.4 g, 71% yield). 1H NMR (400.0 MHz, DMSO-d6) δ 8.11 (s, 1H), 7.95 (s, 1H), 3.88 (s, 3H), 2.25 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367660B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-6b463a950a9c488b8fe064d088814f3e |
| Source note | uspto-grants-2013_02 |