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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21006Generated: October 25, 2026

Dimethylformamide → 4-Chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone

https://huagongshe.com/reaction/21006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant3-chloro-N-(1-methyl-1-phenylethyl)benzamideHCID 47444761—
ReactantHCID 178444656HCID 178444656—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinoneHCID 6849004389%

Reaction Steps

3-Chloro-N-(1-methyl-1-phenylethyl)benzamide (7.00 g, 25.6 mmol) was dissolved in THF (280 mL), and the solution was added with TMEDA (12.4 mL, 81.9 mmol), then added with sec-butyllithium-hexane solution (0.99 mol/L, 82.7 mL, 81.9 mmol) by drops at −78° C. for 40 minutes under argon atmosphere, followed by stirring at the same temperature for 2.5 hours. Then, the mixture was added with DMF (4.36 mL, 56.3 mmol) and warmed from −78° C. to room temperature over 2 hours. The reaction mixture was added with water, extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by slurry using diisopropyl ether to obtain 4-chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone (6.86 g, yield 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-f45e4ddcaba84c37bb2475ecd5f8e92f
Source noteuspto-grants-2010_06