HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 2-Allyloxy-1,4-dinitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 2,5-Dinitrophenol | HCID 9492 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-Allyloxy-1,4-dinitrobenzene | HCID 22251447 | 93.2% |
Reaction Steps
A mixture of 2,5-dinitrophenol (7.36 g, 40 mmol), allyl bromide (4.84 g, 40 mmol), acetone (75 mL), 1-methylpyrrolidinone (3 mL) and potassium carbonate (11.0 g, 80 mmol) was heated to 50–66° C. for 22 h. The mixture was cooled to room temperature and filtered and the solid rinsed with ethyl acetate. The filtrate was concentrated and recrystallized from isopropanol-hexane (1:1) to give 2-allyloxy-1,4-dinitrobenzene as yellow crystals (8.36 g, mp 66.5–68° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06991834B1 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-c5a9e9bb0bd54f8786da0240d07d841b |
| Source note | uspto-grants-2006_01 |