HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → Diethyl 1-(ethyloxy)-4-hydroxy-2,3-naphthalenedicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Diethyl 1,4-dihydroxy-2,3-naphthalenedicarboxylate | HCID 43109 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Diethyl 1-(ethyloxy)-4-hydroxy-2,3-naphthalenedicarboxylate | HCID 58012479 | 60.5% |
Reaction Steps
Bromoethane (0.359 g, 3.29 mmol) was added to a stirred solution of diethyl 1,4-dihydroxy-2,3-naphthalenedicarboxylate (1 g, 3.29 mmol) and potassium carbonate (0.454 g, 3.29 mmol) in acetone (25 ml). The reaction mixture was refluxed for 24 hours under an atmosphere of argon. The resulting mixture was evaporated and the residue was partitioned between 2× ethylacetate and water. The combined organics were washed with water and dried over magnesium sulphate. The orange oil was purified by chromatography on silica gel, eluting with ethyl acetate (0-10%) in hexane to give the title compound as a clear oil (0.661 g, 1.99 mmol). LC/MS: Rt=3.63, [MH]− 331.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08207213B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-148d4c5c1a5a4172a12879080866651a |
| Source note | uspto-grants-2012_06 |