Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623737Generated: October 30, 2026

Sodium Hydroxide → 1-Benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-2-carboxylic acid

https://huagongshe.com/reaction/623737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-2-carboxylateHCID 86711825—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-2-carboxylic acidHCID 86711827—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ethyl 1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-2-carboxylate (2.59 g, 6.35 mmol) in dry THF (15 mL) was added a solution of NaOH (3.9 g, 98 mmol) in H2O (15 mL). The reaction mixture was stirred overnight at 80° C. An additional portion of NaOH (4.25 g, 106 mmol) was added and the reaction mixture was stirred at 100° C. during 7 h. The organic solvent was evaporated and the residue was acidified with aqueous 5 M HCl (55 mL). The product was extracted with EtOAc (3×20 mL). The combined organic layer was washed with brine (3×20 mL) and dried (Na2SO4). The remaining oil was triturated with heptane (20 mL). The off-white solids were filtered off to give 1.29 g (51%) ACI-06.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302988B2
Source datasetuspto-grants-2016_04
ORD IDord-59e1ed40479844d89bc7654de8e543a8
Source noteuspto-grants-2016_04