HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 2,4-Dibromo-6-methylphenyl 2-methylprop-2-en-1-yl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4-Dibromo-6-methylphenol | HCID 11861 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2,4-Dibromo-6-methylphenyl 2-methylprop-2-en-1-yl ether | HCID 15454074 | — |
Reaction Steps
A solution of 2,4-dibromo-6-methyl-phenol (Compound 3,62 g, 0.23 mol) in 700 mL of acetone was treated with potassium carbonate (38.7 g, 0.28 mol), sodium iodide (3.4 g, 0.023 mol) and 3-chloro-2-methylpropene (34 mL, 0.35 mol) and the resulting suspension was refluxed for 18 hours. The solids were filtered and the filtrate was evaporated in vacuo to afford the title compound as a dark yellow oil. 1H-NMR (300 MHz, CDCl3): δ 7.53(d, 1H, J=2.7 Hz), 7.27(d, 1H, J=1.9 Hz), 5.17(s, 1H), 5.02(s, 1H), 4.28(s, 2H), 2.30(s, 3H), 1.92(s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093838 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-f82c4cb0677f41e2958cc98630730ecb |
| Source note | uspto-grants-2000_07 |