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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31355Generated: October 26, 2026

Ammonium Chloride → 3,5-Dichloro-3-(2-methoxyphenyl)-6-methyl-1,3-dihydro-2h-indol-2-one

https://huagongshe.com/reaction/31355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 2-methoxybenzoylformateHCID 15579652—
Reactanttert-Butyl (4-chloro-3-methylphenyl)carbamateHCID 21905898—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Product3,5-Dichloro-3-(2-methoxyphenyl)-6-methyl-1,3-dihydro-2h-indol-2-oneHCID 21905961—

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of 5 g of tert-butyl 4-chloro-3-methylphenylcarbamate in 45 ml of ether is cooled to −70° C. under an argon atmosphere, 30 ml of a 1.5M solution of tert-butyllithium in pentane are added dropwise, the mixture is left stirring for 1 hour while allowing the temperature to rise to −10° C., and is left stirring for 1 hour 45 minutes at −10° C. The reaction mixture is cooled to −70° C., a solution of 5 g of the compound obtained in step A in 25 ml of THF is added dropwise and the mixture is left stirring for 1 hour while allowing the temperature to rise to −30° C., and is then stirred overnight while allowing the temperature to rise to RT. Saturated NH4Cl solution is added to the reaction mixture, the THF is evaporated off, the resulting aqueous phase is extracted three times with EtOAc, the organic phase is washed with water, with saturated NaCl solution and dried over Na2SO4, the solvent is partially evaporated off and the crystalline product is spin-filtered off. 2.6 g of the expected product are obtained; m.p.=254-256° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425566B2
Source datasetuspto-grants-2008_09
ORD IDord-1ce7539a41534ff092bba385bf3b8874
Source noteuspto-grants-2008_09