HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815462Generated: October 30, 2026
2-Chlorobenzaldehyde → HCID 10636680, compound
https://huagongshe.com/reaction/1815462
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4-Dichlorobenzenethiol | HCID 70730 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10636680 | HCID 10636680 | 83% |
Reaction Steps
To a stirred solution of 2,4-dichlorothiophenol (2.0 g, 11.2 mmol) in 25 mL of anhydrous DMF was added potassium carbonate (3.09 g, 22.4 mmol), followed by 2-chlorobenzaldehyde (1.26 mL, 11.3 mmol). The mixture was then heated under nitrogen atmosphere at 70° C. for 5 hours. The reaction mixture was then allowed to cool to room temperature and partitioned between ether and water. The aqueous layer was extracted with ether once and the combined organic layer was washed with water and brine, dried over sodium sulfate and condensed in vacuo. The crude product was purified via silica gel flash chromatography, eluting with 5-10% ether/hexanes, to give 2.62 g (9.25 mmol, 83%) of the desired aldehyde as a colorless oil, which solidified slowly upon standing at room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06878700B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-47645eb930d145a9a0b0cc1f036ac41a |
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| Source note | uspto-grants-2005_04 |
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