HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2719Generated: October 23, 2026
3-Pyridinecarboxaldehyde → Pyridine, 3-(2,2-dibromoethenyl)-
https://huagongshe.com/en/reaction/2719
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Pyridine, 3-(2,2-dibromoethenyl)- | HCID 11334526 | 70% |
Reaction Steps
Tetrabromomethane (24.82 g, 0.747 mole) and triphenylphosphine (39.17 g, 0.149 mole) were stirred together in dry methylene chloride (100 mL) for 5 min. at 0° C. under a nitrogen atmosphere. To this mixture was added dropwise pyridine 3-carboxaldehyde (4 g, 0.0373 mole). The solution was then stirred for 45 min. at ambient temperature. The reaction mixture was extracted with aqueous 6N hydrochloric acid (3×25 mL), the aqueous layer basified with solid sodium bicarbonate to pH 8-9 and extracted with chloroform (4×25 mL). The combined organic liquours were dried over anhydrous sodium sulfate, filtered and concentrated on a rotary evaporator to give a dark colored syrup. The crude product was chromatographed on silica gel (70-230 mesh) with chloroform:methanol (95:5) as eluant, to afford a light yellow solid (5.0 g, 70%) which rapidly turned dark on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05731314 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-d7edba51f018489380d4a887b1e9b6d1 |
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| Source note | uspto-grants-1998_03 |
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