HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880454Generated: October 27, 2026
1,2-Dichloroethane → 1-phenyl-1H-pyrrole-2-carbaldehyde
https://huagongshe.com/reaction/880454
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Phenylpyrrole | HCID 12480 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Product | 1-phenyl-1H-pyrrole-2-carbaldehyde | HCID 934729 | 59% |
Reaction Steps
Phosphorus oxychloride (0.7 mL, 7.68 mmol) was added slowly to ice-cold dimethylformamide (0.6 mL, 7.68 mmol). The mixture was warmed to room temperature and stirred for 15 min. A solution of 1-phenylpyrrole (1.0 g, 6.98 mmol) in ethylene dichloride (5 mL) was added and the reaction mixture heated at reflux for 1 h. The mixture was cooled to 10° C. and quenched into 10% sodium acetate solution (20 mL). The organic layer was separated and the aqueous phase was extracted with ether. The combined organic layers were washed with water, brine, dried over anhydrous sodium sulfate, filtered and concentrated under in vacuo to give a crude residue. Purification by column chromatography over silica gel (60-120 mesh) using 2% ethyl acetate in petroleum ether as eluent gave 1-phenylpyrrole-2-carbaldehyde (700 mg, 59%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993574B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-66e267d473094e30bcbbd712a3c1ef4d |
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| Source note | uspto-grants-2015_03 |
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