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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366947Generated: October 27, 2026

4-Chlorophenylacetyl chloride → 4-[2-(4-Chlorophenyl)-acetyl]-5-methyl-1H-pyrrole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1366947

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorophenylacetyl chlorideHCID 90692—
Reactant1H-Pyrrole-2-carboxylic acid, 5-methyl-, ethyl esterHCID 96598—
Solvent1,2-DichloroethaneHCID 11—
Product4-[2-(4-Chlorophenyl)-acetyl]-5-methyl-1H-pyrrole-2-carboxylic acid ethyl esterHCID 5823145883%

Reaction Steps

4-[2-(4-Chlorophenyl)-acetyl]-5-methyl-1H-pyrrole-2-carboxylic acid ethyl ester (108) was synthesized from 5-methyl-1H-pyrrole-2-carboxylic acid ethyl ester (107) and (4-chlorophenyl)-acetyl chloride following the procedure described in Example 32. Reaction Conditions: 1,2-dichloroethane/RT. Purification: recrystallization from ether/pentane. Yield: 83%. 1H (CDCl3, 400 MHz): δ 9.65 (NH, broad s), 7.28 (3H, m), 7.2 (2H, d), 4.35 (2H, q), 4.04 (2H, s), 2.57 (3H, s), 1.38 (3H, t) ppm. 13C (CDCl3, 100 MHz): δ 193.7, 161.5, 141.0, 133.5, 132.6, 130.9, 130.7, 128.9, 128.6, 121.4, 120.5, 116.9, 61.0, 46.1, 14.4, 14.0 ppm. LC/MS: 100%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893098B2
Source datasetuspto-grants-2011_02
ORD IDord-48698b616dfc4c5dace23d685944eb9b
Source noteuspto-grants-2011_02