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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 6-Methoxy-3-methyl-1,3-dihydro-indol-2-one | HCID 22241538 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Methoxy-3,3-dimethylindolin-2-one | HCID 22241603 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005440B1 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-d257a4a7c4b94205a56784f4e7b3df6e |
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| Source note | uspto-grants-2006_02 |
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