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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951652Generated: November 2, 2026

Dichloromethane → 2-Oxo-1-(4-trifluoromethyl-benzyl)-2,3-dihydro-1H-indole-7-carboxylic acid

https://huagongshe.com/reaction/1951652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant7-Bromo-1-(4-trifluoromethylbenzyl)-1,3-dihydro-indol-2-oneHCID 58297678—
SolventWaterHCID 962—
SolventDimethyl sulfoxide methanolHCID 22036561—
Product2-Oxo-1-(4-trifluoromethyl-benzyl)-2,3-dihydro-1H-indole-7-carboxylic acidHCID 58297700—

Reaction Steps

A mixture 2.8 g of 7-bromo-1-(4-trifluoromethylbenzyl)-1,3-dihydro-indol-2-one, 0.70 g of PdCl2dppf.CH2Cl2, and 2.34 ml of Et3N in 75 ml of 2:1 DMSO/MeOH was heated under CO (balloon pressure) at 75° C. for 24 h. The reaction mixture was poured into 400 ml of 1:1 heaxan/EtOAc and stirred with 200 ml of water for 4 h. The organic layer was washed with 150 ml of brine and dried over Na2SO4, filtered through a pad of silica gel, and concentrated. The residue was dissolved in 60 ml THF, 20 ml of MeOH and 20 ml of water, followed by 30 ml of 1N aqueous LiOH solution. After stirring for 5 h at room temperature, 5 ml of AcOH was added and the mixture was extracted with 250 ml of EtOAc. The organic layer was washed with 50 ml of brine and dried over Na2SO4, filtered, and concentrated. The residue was swished from 50 ml of 1:1 hexane/EtOAc to give 1.2 g of the title compound as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404736B2
Source datasetuspto-grants-2013_03
ORD IDord-b9dfcc9a1b9e474f8e4465e9589406b0
Source noteuspto-grants-2013_03