HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dibromoethane → 1-(2-Bromoethoxy)-3,5-dichlorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | 3,5-Dichlorophenol | HCID 11571 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(2-Bromoethoxy)-3,5-dichlorobenzene | HCID 22246776 | 45.7% |
Reaction Steps
To a solution of NaOH (2.45 g, 61.3 mmol) in water (20 mL) was added 3,5-dichlorophenol (5 g, 30.7 mmol). The solution was heated at reflux for 1 h and was cooled to room temperature. Dibromoethane (11.52 g, 61.3 mmol) was added and the reaction was heated at reflux for 24 h. The cooled solution was diluted with EtOAc and the organic solution was washed sequentially with HCl (1N, 1×), water (1×), and brine (1×). The organic solution was dried (MgSO4), filtered, and concentrated. Purification by flash chromatography (hexanes to 5% EtOAc in hexanes ) provided the title compound (3.79 g). 1H NMR (400 MHz, CDCl3) δ 6.98 (m, 1H), 6.82 (m, 2H), 4.25 (t, 2H), 3.61 (t, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492412B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-69600e2f4eaf42ae8a6b88bc43095b82 |
| Source note | uspto-grants-2002_12 |