HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Bromide → 2-Bromo-6-ethoxynaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Bromide | HCID 6323 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Bromo-6-ethoxynaphthalene | HCID 236858 | — |
Reaction Steps
This experimental procedure is an O-alkylation. A solution of bromomethane (48.90 g, 0.45 mol) is added dropwise to a stirred refluxing mixture of 6-Bromo-2-naphthol (40.00 g, 0.18 mol) and potassium carbonate (63.00 g, 0.46 mol) in acetone. The stirred mixture is heated under reflux for 24 hours (ie until glc analysis reveals a complete reaction). The potassium carbonate is filtered off, water is added to filtrate and the product is recrystallised from ethanol to give a yield of 43.92 g (97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05820781 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-a2e80eb80d1047d1a23f28aea9355410 |
| Source note | uspto-grants-1998_10 |