HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → 1,3-Dibromo-2-(2-bromoethoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,6-Dibromophenol | HCID 11847 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-Dibromo-2-(2-bromoethoxy)benzene | HCID 29272284 | 57% |
Reaction Steps
1,2-Dibromoethane (5.0 ml, 58 mmol) was added to a solution of sodium hydroxide (2.5 g, 63 mmol) and 2,6-dibromophenol (14.5 g, 57.6 mmol) in 45 ml of water. The mixture was stirred under reflux for 20 hours and then extracted with ether. The combined organic layers was dried over Na2SO4, filtered and concentrated to give colorless oil. Silica gel chromatography using a gradient of ethyl acetate in hexanes to afforded 1,3-dibromo-2-(2-bromo-ethoxy)-benzene (11.55 g, 57% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361763B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-b089f108ec334081bf018e2d28244f29 |
| Source note | uspto-grants-2008_04 |