HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → 1,6-Dibromo-2-(2-bromoethoxy)naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Naphthol, 1,6-dibromo- | HCID 27768 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,6-Dibromo-2-(2-bromoethoxy)naphthalene | HCID 57845449 | 69.9% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
1,6-Dibromo-2-naphthol (15.0 g, 49.67 mmol) and 1,2-dibromoethane (46.7 g, 248.37 mmol) were added to a suspension of potassium carbonate (84.8 g, 74.51 mmol) in acetonitrile (500 mL) at rt. The reaction mixture was stirred for 48 h. Additional 1,2-dibromoethane (21.5 mL, 248.37 mmol) was added and the reaction mixture was stirred for 96 h at rt. The reaction mixture was cooled to 0° C. with an ice bath and filtered through a fritted glass funnel. The resulting filtrate was concentrated under reduced pressure to give the title compound (14.2 g, 69.9% yield) as a brown solid. GC/MS m/z 406 (M)+, RT 10.25 min; 1H NMR (400 MHz, acetone-d6) δ 14-8.09 (m, 2H), 7.96 (d, 1H), 7.71 (d, 1H), 7.54 (d, 1H), 4.64-4.60 (m, 2H), 3.90-3.86 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592361B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-26be35a68e7d47ae8aa3bb0fd838b34b |
| Source note | uspto-grants-2009_09 |