HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282335Generated: November 1, 2026
4-Nitrobenzoyl chloride → HCID 18424304, compound
https://huagongshe.com/reaction/1282335
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | 1H-Pyrrole-2-acetic acid, 1-methyl-, ethyl ester | HCID 97469 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18424304 | HCID 18424304 | — |
Reaction Steps
A solution of 5.5 g. (0.03 mole) of p-nitrobenzoyl chloride in 60 ml. methylene chloride is added to a suspension of 3.9 g. (0.03 mole) aluminum chloride in 20 ml. methylene chloride. The resulting suspension is added dropwise to a chilled (−15° C.) solution of ethyl 1-methylpyrrole-2-acetate in 50 ml. methylene chloride. The solution is stirred for 15 minutes at −10° C. and at room temperature for 15 minutes. The reaction mixture is poured into ice-dilute hydrochloric acid. The organic phase is separated and washed successively with N,N-dimethyl-1,3-propanediamine, 3N hydrochloric acid and a saturated solution of sodium chloride, dried over anhydrous magnesium sulfate, and the solvent evaporated in vacuo. A solid, ethyl 5-(p-nitrobenzoyl)-1-methylpyrrole-2-acetate, crystallizes from the remaining oily residue which is isolated by recrystallization from methanol, m.p. 103-106° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06455703B2 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-1f16641a1e79435a8179e34aed8fec25 |
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| Source note | uspto-grants-2002_09 |
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