HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 18782518, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenol, 2-bromo-4-(2,2,2-trifluoroethoxy)- | HCID 18782560 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 18782518 | HCID 18782518 | — |
Reaction Steps
To a solution of 2-bromo-4-(2,2,2-trifluoroethoxy)phenol (Description 20, 0.6 g) in acetone was added added K2CO3 (1 g) and methyl iodide (1 ml). The solution was heated to reflux for 1 h. and then evaporated in vacuo. The residue was partitioned between ethyl acetate and water and the organic phase washed further with water and saturated brine. After drying (MgSO4) the solvent was removed in vacuo to give the title compound as a yellow oil. 1H NMR (250 MHz, CDCl3) δ3.87 (3H, s) 4.30 (2H, q, J 8 Hz), 6.82-6.92 (2H, m), and 7.20 (1H, d, J 3 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06071927 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-cf82aac6c4754cae93eaf342eebef1a8 |
| Source note | uspto-grants-2000_06 |