HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42639Generated: October 28, 2026
Sodium Carbonate → HCID 68702253, compound
https://huagongshe.com/reaction/42639
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(Benzyloxy)-3-methoxybenzeneboronic acid | HCID 10682603 | — |
| Reactant | 2-(3-Bromophenyl)-6-(trifluoromethyl)pyridine | HCID 68699540 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68702253 | HCID 68702253 | — |
Reaction Steps
To a stirred solution of 4-benzyloxy-3-methoxyphenylboronic acid (1.0 g, 3.87 mmol) and 2-(3-bromophenyl)-6-(trifluoromethyl)pyridine (1.063 g, 3.52 mmol) in toluene (10 mL) and ethanol (1 mL) at room temperature under argon was added 2 N aqueous sodium carbonate solution (5.41 mL, 10.82 mmol) followed by tetrakis(triphenylphosphine)palladium (0.22 g, 0.19 mmol). The resulting mixture was stirred at 90° C. for two hours and then allowed to cool to room temperature. The phases were separated and the aqueous phase was extracted with toluene (5 mL). The combined organic phases were washed with water and brine, then dried over anhydrous sodium sulphate and filtered. Evaporation of the solvent left a brown oil that was chromatographed over silica gel (petroleum ether/ethyl acetate, 9:1) to give 2-(4′-(benzyloxy)-3′-methoxybiphenyl-3-yl)-6-(trifluoromethyl)pyridine as a clear oil, 1.072 g (70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08536203B2 |
|---|
| Source dataset | uspto-grants-2013_09 |
|---|
| ORD ID | ord-6bab21e86d3a41eb84ffbded31c6ce62 |
|---|
| Source note | uspto-grants-2013_09 |
|---|