HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → Methyl 1-methoxy-4-bromo-2-naphthoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-1-hydroxynaphthalene-2-carboxylic acid | HCID 289393 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 1-methoxy-4-bromo-2-naphthoate | HCID 12084039 | — |
Reaction Steps
To a solution of 4-bromo-1-hydroxy-2-naphthoic acid (see Example 1, 1.63 g, 6.10 mmol) in 35 mL of acetone was added dimethyl sulfate (1.75 mL, 18.3 mmol) and potassium carbonate (2.95 g, 21.4 mmol). The reaction was heated to reflux for 14 hours, cooled to room temperature, filtered, and concentrated in vacuo. The residue was purified via silica gel chromatography, eluting with 0-20% ethyl acetate in hexanes to provide methyl 4-bromo-1-methoxy-2-naphthoate that gave a proton NMR spectra consistent with theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883850B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-a51ff0d38edf42aba92bee747b035f5f |
| Source note | uspto-grants-2014_11 |