HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → Diethyl 2,5-dinaphth-1-ylterephthalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Naphthaleneboronic acid | HCID 254532 | — |
| Reactant | Diethyl dibromoterephthalate | HCID 66645638 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Diethyl 2,5-dinaphth-1-ylterephthalate | HCID 57782612 | — |
Reaction Steps
193.3 g (0.82 mol) of naphthylboronic acid, 180.4 g (474 mmol) of diethyl dibromoterephthalate and 315.9 g (2-29 mol) of potassium carbonate are initially introduced in a mixture of 850 ml of toluene and 850 ml of water and saturated with N2 for 30 min. After addition of 1.36 g (1.18 mmol) of Pd(PPh3)4, the mixture is heated at the boil for 4 h. After cooling to RT and addition of 400 ml of EtOH, the mixture is cooled to room temperature and stirred for 1 h, and the precipitate is filtered off with suction, washed with water, EtOH and heptane and dried at 80° C. in vacuo. The yield of colourless solid is 160.7 g (71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08932732B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-b31f1387ddfb4ff4887bebc258b802c2 |
| Source note | uspto-grants-2015_01 |