HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthol → 1-(2-Bromoethoxy)naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium naphthalate | HCID 23664128 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(2-Bromoethoxy)naphthalene | HCID 11075906 | 50.3% |
Reaction Steps
A solution of 144.0 g (1 mole) α-naphthol and 56.1 g (1 mole) potassium hydroxide in 600 ml of 95% ethanol was stirred 1.5 hr at room temperature. To this solution of potassium naphthalate was added 930.0 g (5.0 mole) of 1,2-dibromoethane, and the solution was heated at reflux overnight. The reaction mixture was filtered, and the filtrate stripped to dryness under reduced pressure in a rotary evaporator. The resulting oil was dissolved in chloroform and the solution extracted with 10% aqueous sodium hydroxide. The chloroform layer was dried and stripped of chloroform to yield 126 g (50.3%) of dark brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04500529 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-e126e237c225482f838909074476a55e |
| Source note | uspto-grants-1985_02 |