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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908240Generated: October 31, 2026

Hydrochloric Acid → 4-(2,4,6-Trifluorobenzoyl)-1H-pyrrole-2-carboxylic acid

https://huagongshe.com/reaction/908240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyrrole-2-Carboxylic AcidHCID 12473—
Reactant2,4,6-Trifluorobenzoyl chlorideHCID 144895—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product4-(2,4,6-Trifluorobenzoyl)-1H-pyrrole-2-carboxylic acidHCID 5340257897.9%

Reaction Steps

To a 120 mL DCM solution of 2,4,6-trifluorobenzoyl chloride (4.3 g, 0.022 mol) was added AlCl3 (8.8 g, 0.066 mol) under N2 at room temperature. After stirring for 15 min, 1H-pyrrole-2-carboxylic acid (2.4 g, 0.022 mol) was added in small portions over a 10 min period. After stirring at room temperature for 1 hr, the reaction mixture was treated with dropwise addition of ice-water (20 mL) and 1N HCl to adjust pH to 1, stirred for another 30 min, extracted with EtOAc (3×30 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated to give the title compound (5.8g, 97% yield). 1H-NMR (500 MHz, CDCl3): δ 12.48 (br.s, 1H), 7.48 (s, 1H), 7.28-7.38 (m, 2H), 6.83 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017605B2
Source datasetuspto-grants-2011_09
ORD IDord-dd7f9ce25bc344f8a8141444d7bef9a8
Source noteuspto-grants-2011_09