HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117207Generated: October 30, 2026
Methyl iodide → 6-Methoxy-3-methyl-1,3-dihydro-indol-2-one
https://huagongshe.com/reaction/2117207
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 6-Methoxyoxindole | HCID 2793749 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Methoxy-3-methyl-1,3-dihydro-indol-2-one | HCID 22241538 | — |
Reaction Steps
To a cooled solution (−78° C.) of 6-methoxy-1,3-dihydro-indol-2-one (840 mg, 5.2 mmol, see Quallich, G. J.; Morrissey, P. M. Synthesis 1993, 51-53) in THF (20 mL) is added dropwise TMEDA (1.57 mL, 10.4 mL) followed by dropwise addition of 2.5M n-BuLi (4.16 mL, 10.4 mmol). The mixture is stirred for 15 min then warmed to −25° C. Add dropwise iodomethane (405 μL, 6.5 mmol) and let stir for 20 min. The reaction is quenched with sat NH4Cl soln, warmed to room temp and diluted with EtOAc. The organic layer is washed with sat NH4Cl soln, brine, dried over MgSO4 and concentrated. The residue is purified by flash chromatography (eluting with 45% ethyl acetate/hexanes) to give 679 mg of title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE040558E1 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-148e97211f1c41a3904f906ac4e1cf3c |
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| Source note | uspto-grants-2008_10 |
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