HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622557Generated: October 25, 2026
Citric Acid → 3-Bromopyridine-2-carbaldehyde
https://huagongshe.com/reaction/1622557
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | 3-bromo-2-(dibromomethyl)Pyridine | HCID 86072544 | — |
| Solvent | Morpholine | HCID 8083 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Bromopyridine-2-carbaldehyde | HCID 16414231 | — |
Reaction Steps
A suspension of 3-bromo-2-dibromomethyl-pyridine (10.0 g, 30.32 mmol) in morpholine (30.0 mL) was heated at 60° C. for 1 h. The reaction mixture was then cooled to rt and diluted with EtOAc (200 mL) followed by adjustment to pH 4 by adding citric acid (40.0 g). The reaction mixture was extracted with EtOAc (3×200 mL). The combined organic layers were dried over Na2SO4 and concentrated under reduced pressure. The resulting residue was purified by column chromatography using silica (100-200 mesh) and 3% EtOAc in hexane as eluent to give 3-bromo-pyridine-2-carbaldehyde. 1H-NMR (400 MHz, CDCl3) δ ppm 10.23 (s, 1H), 8.75 (d, 1H), 8.03 (d, 1H), 7.32 (t, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08778941B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-b7e36e7bd7e14790ad776dd7d16178dd |
|---|
| Source note | uspto-grants-2014_07 |
|---|