HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606178Generated: October 30, 2026
4-Fluorobenzoyl chloride → HCID 18424154, compound
https://huagongshe.com/reaction/1606178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | Ethyl 1,4-dimethyl-1H-pyrrole-2-acetate | HCID 118467 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 18424154 | HCID 18424154 | 25% |
Reaction Steps
A solution of 3.95 g. (0.025 mole) of p-fluorobenzoyl chloride and 3.32 g. (0.025 mole) of aluminum chloride in 20 ml. of 1,2-dichloroethane is added dropwise to a solution of 4.52 g. (0.025 mole) of ethyl 1,4-dimethylpyrrole-2-acetate in 20 ml. of 1,2-dichloroethane at room temperature. The reaction mixture is stirred for 2 hrs. and then cooled and poured into ice-dilute HCl. The organic phase is separated and washed successively with N,N-dimethyl-1,3-propanediamine, dilute hydrochloric acid and a saturated solution of sodium chloride; dried over anhydrous magnesium sulfate; and the solvent evaporated. The residue is triturated with hot hexane and crystals form upon cooling. There is obtained about 1.9 g. (25% yield) of ethyl 1,4-dimethyl-5-(p-fluorobenzoyl)-pyrrole-2-acetate as a white solid, m.p. 84°-86°C. Upon recrystallization from methanol, the m.p. is 87°-89°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03952012 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-cb211e45b5c240efb18d5b87e61ff3c0 |
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| Source note | uspto-grants-1976_04 |
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