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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407378Generated: October 27, 2026

Sodium hydride → 4-chloro-1-(diphenylmethyl)-1H-indole-2,3-dione

https://huagongshe.com/reaction/1407378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-ChloroisatinHCID 96047—
ReactantBromodiphenylmethaneHCID 236603—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-chloro-1-(diphenylmethyl)-1H-indole-2,3-dioneHCID 6735655481.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-chloroisatin (9.10 g, 50.0 mmol) in N,N-dimethylformamide (100 mL) was added sodium hydride (2.20 g, 55.0 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 1 h, followed by the addition of bromodiphenylmethane (14.80 g, 56.8 mmol). The mixture was stirred at ambient temperature for 20 h, diluted with ethyl acetate, washed with water and brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo. The residue was recrystallized from diethyl ether and hexanes to afford 4-chloro-1-(diphenylmethyl)-1H-indole-2,3-dione (14.20 g, 81%): 1H NMR (300 MHz, CDCl3) δ7.37-7.17 (m, 11H), 6.98-6.95 (m, 2H), 6.42 (d, J=9.0 Hz, 1H); MS (ES+) m/z 369.9 (M+23), 371.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916580B2
Source datasetuspto-grants-2014_12
ORD IDord-3960b87b73b14458af0e04c6ab3d0586
Source noteuspto-grants-2014_12