HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482032Generated: October 25, 2026
1,2-Dichloroethane → 3,4-dimethyl-1H-pyrrole-2-carboxaldehyde
https://huagongshe.com/reaction/482032
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3,4-Dimethylpyrrole | HCID 5324584 | — |
| Product | 3,4-dimethyl-1H-pyrrole-2-carboxaldehyde | HCID 579626 | 50% |
Reaction Steps
To a solution of 0.92 mL (12 mmoles) of N,N-dimethylformamide in mL of 1,2-dichloroethane was added dropwise 1.0 mL (12 mmoles) of phosphorus oxychloride at 0°C. The ice-bath was removed and the reaction mixture was further stirred for 30 min. 3,4-Dimethylpyrrole (960.0 mg, 10 mmoles) was added to the above solution portionwise and the reaction mixture was stirred at 50° C. for 5 h. The reaction mixture was poured into ice-cold 1N sodium hydroxide solution (pH=9 after mixing) and the resulting mixture was stirred at room temperature for 1 h. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with brine until pH=7, dried over anhydrous sodium sulfate and evaporated. The residue was chromatographed on a silica gel column eluting with a solvent mixture of ethyl acetate and hexane to afford 610 mg (50%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05792783 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-f8448572e84d42ae8d3459ece5e34daa |
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| Source note | uspto-grants-1998_08 |
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