HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 22477865, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3,4-Dinitrophenol | HCID 11348 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22477865 | HCID 22477865 | — |
Reaction Steps
A stirred solution of 3,4-dinitrophenol (1 g) in dimethylformamide (30 mL) was treated with benzyl bromide (723 μL) and potassium carbonate (1.13 g). The reaction mixture was stirred at ambient temperature for 24 hours and then partitioned between ethyl acetate and water. The organic layer was washed with brine, then dried over magnesium sulfate and then evaporated. The residue was subjected to flash column chromatography on silica eluting with a mixture of ethyl acetate and hexane (1:4, v/v) to give 4-benzyloxy-1,2-dinitrobenzene (1.30 g) as a yellow solid. LC-MS (METHOD B): RT=3.31 minutes. 1H NMR [(CD3)2CO, ppm): δ 5.28 (s, 2H), 7.26-7.42 (m, 6H), 7.57 (d, 1H), 8.12 (d, 1H). (b) 1-Ethyl-2-methoxy-benzene
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06897208B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-8927ca984b85410aa0ece43d1e03b752 |
| Source note | uspto-grants-2005_05 |