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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24794Generated: October 26, 2026

N-Methyloxindole → HCID 178481538, compound

https://huagongshe.com/reaction/24794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethyloxindoleHCID 6096—
ReactantBenzoyl chlorideHCID 7412—
ReactantDiisopropylamineHCID 7912—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178481538HCID 178481538—

Reaction Conditions

Temperature-70 °C

Reaction Steps

4.15 g (41 mmol) of diisopropylamine are placed in 50 ml of THF, cooled to −70° C. and combined with a solution of 14.4 ml of (36 mmol) of n-butyl lithium solution (2.5 mol in toluene) and stirred for 10 minutes. Then a solution of 5.0 g (34 mmol) of 1-methyl-2-indolinone in 30 ml of THF is added dropwise and stirred for 45 minutes at −70° C. Then 5.8 g (0.041 mol) of benzoylchloride are added dropwise. The reaction solution is left to heat up slowly within 14 hours. It is then poured onto sodium chloride solution and extracted with ethyl acetate. The combined organic extracts are dried and concentrated by evaporation. The residue is chromatographed on silica gel (dichloromethane/methanol/ammonia=200:8:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855710B2
Source datasetuspto-grants-2005_02
ORD IDord-a1c7c69415544c0fba466205d97cb0f2
Source noteuspto-grants-2005_02