HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612752Generated: October 29, 2026
Toluene → 5-(Pyridin-3-yl)thiophene-2-carbaldehyde
https://huagongshe.com/reaction/612752
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Pyridinylboronic acid | HCID 2734378 | — |
| Reactant | (5-bromothien-2-yl)methanol | HCID 11435467 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(Pyridin-3-yl)thiophene-2-carbaldehyde | HCID 10899427 | 98% |
Reaction Steps
To a mixture of 153 mg (5-bromo-thiophen-2-yl)-methanol, 128 mg pyridine-3-boronic acid, and 64 mg tetrakis(triphenylphosphine) palladium was added solvent (7.3 mL toluene and 3.1 mL methanol) followed by 1.4 mL of 2.5M sodium carbonate and the mixture heated to 80° C. on an oil bath. After 16 hours the mixture was cooled to room temperature and cocncentrated in vacuo. The residue was solvated in ethyl acetate was washed sequentially with 0.5N sodium hydroxide and brine, dried over magnesium sulfate and concentrated in vacuo. Purification by flash chromatography on silica gel (hexane:ethyl acetate, 60:40; then 55:45) gave the title compound (147 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06004984 |
|---|
| Source dataset | uspto-grants-1999_12 |
|---|
| ORD ID | ord-75132a495bef401fbc9af96aaf4a8506 |
|---|
| Source note | uspto-grants-1999_12 |
|---|