HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Diethyl 2,2''-dimethyl[1,1';4',1'']terphenyl-2',5'-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methylphenyl boronic acid | HCID 2733267 | — |
| Reactant | Diethyl dibromoterephthalate | HCID 66645638 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Diethyl 2,2''-dimethyl[1,1';4',1'']terphenyl-2',5'-dicarboxylate | HCID 58232266 | — |
Reaction Steps
60 g (160 mmol) of diethyl dibromoterephthalate, 43 g (320 mmol) of o-tolylboronic acid, 365 mg (0.32 mmol) of Pd(PPh3)4 and 92 g (660 mmol) of K2CO3 are heated at the boil for 4 h in 300 ml of toluene and 300 ml of water. The mixture is subsequently partitioned between toluene and water, and the organic phase is washed three times with water and dried over Na2SO4. The residue remaining is recrystallised twice from heptane to give colourless crystals. The yield is 51 g (127 mmol, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08766001B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-9dbfa2f8e87f47028affc398834118b8 |
| Source note | uspto-grants-2014_07 |