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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514266Generated: October 25, 2026

Water → 6-chloro-2-({2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}carbamoyl)-1H-indole-5-carboxylic acid

https://huagongshe.com/reaction/514266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBoron tribromideHCID 25134—
ReactantEthyl 6-chloro-2-({2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}carbamoyl)-1H-indole-5-carboxylateHCID 58247983—
SolventDichloromethaneHCID 6344—
Product6-chloro-2-({2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}carbamoyl)-1H-indole-5-carboxylic acidHCID 8671398479.6%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Ethyl 6-chloro-2-({2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}carbamoyl)-1H-indole-5-carboxylate (2.90 g, 5.0 mmol, 85% pure) was dissolved in 5 ml of dichloromethane and a solution of boron tribromide in dichloromethane (27.5 ml, 27.5 mmol) was added dropwise at −10° C. The reaction mixture was stirred at −10° C. for 1 h and then at room temperature for 2 h. Water was added and the precipitated solid was filtered off with suction and dried. 1.85 g (79% of theory) of 6-chloro-2-({2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}carbamoyl)-1H-indole-5-carboxylic acid were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09107411B2
Source datasetuspto-grants-2015_08
ORD IDord-1845da64d6b0495583bfd9c4128e84ae
Source noteuspto-grants-2015_08