Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Hydroxynaphthalen-3,6-dicarboxylic acid | HCID 9816055 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21191987 | HCID 21191987 | 134.8% |
Reaction Steps
2-Hydroxy-3,6-di-hydroxycarbonylnaphthalene (2.4 g) was dissolved in dimethylformamide (50 g), followed by heating to 100° C. Potassium carbonate (4.6 g) was slowly added and benzyl chloride (4.2 g) was added dropwise. After heating for about 20 hours, the reaction solution was poured into a mixed solution of water (300 g) and methanol (100 g). The deposit was filtered and then washed with water to obtain 3.5 g of 2-benzyloxy-3,6-di-benzyloxycarbonylnaphthalene as whitish yellow powder (DSC analysis value: 100.5° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05786523 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-0589e8a87c0d414a8be0d044a89a43d3 |
|---|
| Source note | uspto-grants-1998_07 |
|---|
