HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377726Generated: October 26, 2026
Methyl iodide → 4-Benzyloxy-2-methoxybenzoic acid methyl ester
https://huagongshe.com/reaction/1377726
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 4-(benzyloxy)-2-hydroxybenzoate | HCID 225489 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Benzyloxy-2-methoxybenzoic acid methyl ester | HCID 10826039 | 90% |
Reaction Steps
To a solution of methyl 2-hydroxy-4-benzyloxybenzoate (50 g, 194 mmol) in dry DMF (500 mL) was added methyl iodide (30 mL, 2.5 eq) and the solution was cooled to 0° C. under argon. The solution was stirred at 0° C. and sodium hydride (60% dispersion in mineral oil, 12 g, 1.5 eq) was added in several portions over 15 minutes. The reaction was allowed to warm to ambient temperature with stirring over 18 hours. The reacton was quenched with 12 mL of acetic acid and the solvent was removed under reduced pressure. The residue was partitioned between methylene chloride (700 mL) and saturated sodium bicarbonate (700 mL) and the organic layer was washed with water (2×700 mL), brine, dried over MgSO4, and filtered. The solvent was removed under reduced pressure to give methyl 2-methoxy-4-benzyloxybenzoate as a crystalline solid in 90% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05665719 |
|---|
| Source dataset | uspto-grants-1997_09 |
|---|
| ORD ID | ord-beb6581d8b99425d8bbc2e3dd7e0ae1e |
|---|
| Source note | uspto-grants-1997_09 |
|---|