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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282335Generated: November 1, 2026

4-Nitrobenzoyl chloride → HCID 18424304, compound

https://huagongshe.com/reaction/1282335

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactant1H-Pyrrole-2-acetic acid, 1-methyl-, ethyl esterHCID 97469—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductHCID 18424304HCID 18424304—

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455703B2
Source datasetuspto-grants-2002_09
ORD IDord-1f16641a1e79435a8179e34aed8fec25
Source noteuspto-grants-2002_09