HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509327Generated: October 25, 2026
Citric Acid → 3-Bromopyridine-2-carbaldehyde
https://huagongshe.com/reaction/509327
Participants
| Role | Name | HCID | Charge |
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| 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 mmole) in morpholine (30.0 mL) was heated to 60° C. for 1 h. The reaction mixture was cooled to rt and diluted with EtOAc (200 mL). The pH was adjusted to 4.0 by adding citric acid (40.0 g). The reaction mixture was then extracted with EtOAc (3×200 mL) and the combined organic layers were dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography using silica (100-200 mesh) using 3% EtOAc in hexane as eluent to give 3-bromo-pyridine-2-carbaldehyde. 1H-NMR (400 MHz, CDCl3): c 10.23 (s, 1H), 8.74-8.76 (d, 1H), 8.02-8.04 (d, 1H), 7.26-7.38 (t, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096527B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-496c42a16afb4affbac7088b8bc558f5 |
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| Source note | uspto-grants-2015_08 |
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