HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → 1-(2-Bromoethoxy)-4-(trifluoromethoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | p-(Trifluoromethoxy)phenol | HCID 70015 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(2-Bromoethoxy)-4-(trifluoromethoxy)benzene | HCID 13672274 | 52.1% |
Reaction Steps
To a solution of 4-(trifluoromethoxy)phenol (1 g, 5.61 mmole) in CH3CN (20 mL) was added Cs2CO3 (3.66 g, 11.23 mmole) then 1,2-dibromoethane (2.42 mL, 28.1 mmole). The mixture was heated to reflux. After 3 days the mixture was cooled to RT, filtered through a pad of Celite washing with CH2Cl2, and concentrated. Flash column (Biotage-SNAP-50 g SiO2, 0-10% EtOAc/hexanes) gave the title compound (833 mg, 52%) as a clear liquid. 1H NMR (400 MHz, CDCl3): δ 7.15 (d, J=8.7 Hz, 2 H); 6.95-6.88 (m, 2 H); 4.29 (m, 2 H); 3.64 (t, J=6.29 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09102673B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-14c2497243e24e2ba0997c4838785ae6 |
| Source note | uspto-grants-2015_08 |