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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 7-Bromo-1-(4-trifluoromethylbenzyl)-1,3-dihydro-indol-2-one | HCID 58297678 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethyl sulfoxide methanol | HCID 22036561 | — |
| Product | 2-Oxo-1-(4-trifluoromethyl-benzyl)-2,3-dihydro-1H-indole-7-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404736B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-b9dfcc9a1b9e474f8e4465e9589406b0 |
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| Source note | uspto-grants-2013_03 |
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