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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178116Generated: November 2, 2026

Glycine ethyl ester → Ethyl 4-phenyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1178116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycine ethyl esterHCID 12176—
ReactantPerchlorateHCID 123351—
Reactant(3-Dimethylamino-2-phenyl-allylidene)-dimethyl-ammoniumHCID 3268880—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthyl 4-phenyl-1H-pyrrole-2-carboxylateHCID 1464381331.83%

Reaction Steps

Sodium metal (119 mg, 5.1 mmol) was added to EtOH (15 mL) and stirred for 30 minutes. Glycine ethyl esater hydrochloride (345 mg, 2.47 mmol) and (3-dimethylamino-2-phenyl-allylidene)-dimethyl-ammonium; perchlorate (500 mg, 1.65 mmol) was then added. The resulting mixture was stirred and heated to reflux for 2 hrs. Evaporated the reaction mixture to get the residue. The residue was diluted with cold water and extracted with EtOAc. The organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure to get the residue. The residue obtained was purified by column chromatography (using silicagel of 60-120 mesh and 10% EtOAc in Hexane as eluent) to afford 113 mg (31.83% yield) of 4-phenyl-1H-pyrrole-2-carboxylic acid ethyl ester. LCMS Purity: 98.96%. 1H NMR (CDCl3): δ 9.2 (bs, 1H), 7.58 (d, 2H), 7.42 (t, 2H), 7.26 (m, 3H), 4.4 (q, 2H), 1.4 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-0e33696426fe466abba743dc17e179dd
Source noteuspto-grants-2010_11