Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892201Generated: October 28, 2026

Methyl iodide → 6-Methoxy-3,3-dimethylindolin-2-one

https://huagongshe.com/reaction/892201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant6-Methoxy-3-methyl-1,3-dihydro-indol-2-oneHCID 22241538—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product6-Methoxy-3,3-dimethylindolin-2-oneHCID 22241603—

Reaction Conditions

Temperature-25 °C

Reaction Steps

To a cooled solution (−78° C.) of 6-methoxy-3-methyl-1,3-dihydro-indol-2-one (679 mg, 3.83 mmol, example 77) in THF (13 mL) is added TMEDA (1.16 mL, 7.66 mmol) followed by dropwise addition of 2.5M n-BuLi (3.06 mL, 7.66 mmol). The mixture is stirred 15 min then warmed to −25° C. Iodomethane (275 μL, 4.40 mmol) is added dropwise and stirred for 30 min. Reaction is quenched with sat NH4Cl soln, warmed to room temp and diluted with EtOAc. Washed organic layer with sat NH4Cl soln, brine, dried over MgSO4 and concentrated. The residue is purified by flash chromatography (silica, 35% ethyl acetate in hexanes) to give the title compound as a white crystalline solid. MS (ESI) 192 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07005440B1
Source datasetuspto-grants-2006_02
ORD IDord-d257a4a7c4b94205a56784f4e7b3df6e
Source noteuspto-grants-2006_02