HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613642Generated: October 26, 2026
2-Chlorobenzaldehyde → 1-(Pyrid-3-yl)-2-(2-chlorophenyl)-2-hydroxyethanone
https://huagongshe.com/reaction/1613642
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Catalyst | 3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide | HCID 9964923 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(Pyrid-3-yl)-2-(2-chlorophenyl)-2-hydroxyethanone | HCID 19774206 | — |
Reaction Steps
160 g (1.14 mol) of 2-chlorobenzaldehyde, 122 g (1.14 mol) of 3-pyridinealdehyde, 50 g (0.2 mol) of 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazoliumbromide and 60.6 g (0.6 mol) of triethylamine in one liter of ethanol were heated at 75° C. for 13 hours. Thereafter, the ethanol was distilled off and the residue was dissolved in methylene chloride. The solution was washed twice with water and then extracted twice with 300 ml of 4N hydrochloric acid. The acidic aqueous phase was then rendered slightly alkaline with 4N sodium hydroxide solution and extracted three times with fresh methylene chloride. After the solvent had been distilled off, the crude product was stirred with isopropanol, filtered off under suction and dried to give a product of melting point 92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05194441 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-908219f3f9f24b2c9752eef9575872a0 |
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| Source note | uspto-grants-1993_03 |
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