HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Ethyl 1,4-dihydroxynaphthalene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Naphthalenecarboxylic acid, 1,4-dihydroxy-, phenyl ester | HCID 604249 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 1,4-dihydroxynaphthalene-2-carboxylate | HCID 12388086 | — |
Reaction Steps
28 g of 2-phenoxycarbonyl-1,4-dihydroxynaphthalene was dissolved in ethanol under a nitrogen stream, and 20.4 g of sodium ethylate was added thereto, followed by refluxing for 5 hours under heating. After being cooled, the solution was made weakly acidic with acetic acid, then ethanol was distilled off. Ethyl acetate and water were added thereto to separate and extract the product. The product was purified through silica gel column chromatography with an element having the same composition as that used in the Synthesis Example 1 to obtain compound (6) as crytals. Yield: 13 g (56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04636456 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-33f842f66bb74f2aa01e9a5fa2a63fb6 |
| Source note | uspto-grants-1987_01 |