HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630405Generated: October 26, 2026
Toluene → 5-(3-Fluorophenyl)pyridine-2-carbaldehyde
https://huagongshe.com/reaction/1630405
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Fluorophenylboronic acid | HCID 2733986 | — |
| Reactant | 5-Bromopyridine-2-carbaldehyde | HCID 9877562 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(3-Fluorophenyl)pyridine-2-carbaldehyde | HCID 46313112 | — |
Reaction Steps
A mixture of 2 g of 5-bromopyridine-2-carbaldehyde, 1.96 g of 3-fluorophenylboronic acid, 11.2 g of K2CO3, 160 ml of toluene, 60 ml of water, 60 ml of ethanol and 0.93 mg of tetrakis(triphenylphosphine)palladium (0) is stirred at 100° C. under argon for 2 hours. The solvents are evaporated and the residue is dispersed in 100 ml of water, and the product is extracted with 2 portions of 30 ml of ethyl acetate. The organic phase is washed with 30 ml of sat. brine, dried over sodium sulfate and concentrated. The resulting residue is recrystallized from 28 ml of isopropanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791133B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-419c36b3ccb74bce93aee6fa046a0ea0 |
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| Source note | uspto-grants-2014_07 |
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