HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Dimethyl 1,4,5,8-tetrakis(phenylmethoxy)-2,3-naphthalene dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19808875 | HCID 19808875 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Dimethyl 1,4,5,8-tetrakis(phenylmethoxy)-2,3-naphthalene dicarboxylate | HCID 438021 | — |
Reaction Steps
A mixture of 10.00 g of dimethyl 1,4-dihydroxy-5,8-bis(phenylmethoxyl)-2,3-naphthalene dicarboxylate prepared in Step 2A-b above, 12.00 g of potassium carbonate and 8.0 mL of benzyl bromide in 100 mL of dimethyl formamide and 200 mL of acetone was stirred at room temperature for 2 days. The reaction was filtered. The filtrate was then concentrated and the solid was washed with mixed solvent of ethyl acetate and petroleum ether to give 12.50 g of the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05166208 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-089ca9c6fbb94e4b9196868f68276079 |
| Source note | uspto-grants-1992_11 |