HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275296Generated: October 31, 2026
4-Chlorobenzoyl chloride → HCID 86584041, compound
https://huagongshe.com/reaction/1275296
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 18424250 | HCID 18424250 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 86584041 | HCID 86584041 | — |
Reaction Steps
A solution of 13.8 g. (0.0788 mole) of p-chlorobenzoyl chloride and 10.5 g. (0.0788 mole) of aluminum chloride in 120 ml. of 1,2-dichloroethane is added to a refluxing solution of 21.8 g. (0.0788 mole) of ethyl 3-ethoxycarbonyl-4-ethyl-1-methylpyrrole-2-acetate. The mixture is heated under reflux for 10 hours and stirred at room temperature for an additional 10 hours. It is then poured into ice-hydrochloric acid. The organic layer is separated, and the aqueous layer washed with 1,2-dichloroethane. The combined organics are washed successively with water, N,N-dimethylaminopropylamine, dilute HCl and brine. The solution is then dried over anhydrous magnesium sulfate and the solvent evaporated in vacuo. The residual red oily residue crystallizes on standing. It is recrystallized twice from methanol to give ethyl (5-chlorobenzoyl)-3-ethoxycarbonyl-4-ethyl-1-methyl-pyrrole-2-acetate as a white solid, m.p. 72-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06160003 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-50887931f648492781933cfa317f78aa |
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| Source note | uspto-grants-2000_12 |
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