HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dihydroxynaphthalene → [(4-Hydroxy-2-naphthalenyl)oxy]acetic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dihydroxynaphthalene | HCID 8601 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | [(4-Hydroxy-2-naphthalenyl)oxy]acetic acid methyl ester | HCID 54367121 | 19% |
Reaction Steps
A mixture of 1.5180 g of 1,3-dihydroxynaphthalene and 1.70 g of anhydrous potassium carbonate in 10 ml of anhydrous acetone was stirred at room temperature for 1 hour. Methyl bromoacetate (0.91 ml) was added and stirring at room temperature was continued for 50 hours. The solvent was removed in vacuo and the residue was acidified and extracted with ethyl acetate. The dried (magnesium sulfate) extract was concentrated in vacuo and the product was purified by high pressure liquid chromatography using 20% ethyl acetate-toluene to give 0.419 g (19% yield) of [(4-hydroxy-2-naphthalenyl)oxy]acetic acid methyl ester as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04539419 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-7db0530057b04222a5d4f5243c55694d |
| Source note | uspto-grants-1985_09 |