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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948010Generated: October 30, 2026

Dimethylformamide → 4-Methoxy-2-methyl-7-nitro-2,3-dihydro-isoindol-1-one

https://huagongshe.com/reaction/1948010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hydroxy-2-methyl-7-nitro-2,3-dihydro-isoindol-1-oneHCID 59849205—
SolventEthyl AcetateHCID 8857—
Product4-Methoxy-2-methyl-7-nitro-2,3-dihydro-isoindol-1-oneHCID 5984917950%

Reaction Steps

A mixture of 4-Hydroxy-2-methyl-7-nitro-2,3-dihydro-1H-isoindol-1-one (Compound 205C, 50.0 mg, 0.240 mmol), potassium carbonate (49.8 mg, 0.360 mmol) in DMF (2 mL, 20 mmol) was treated with methyl iodide (22.4 μL, 0.360 mmol) and allowed to stir at room temperature overnight. The reaction was poured into EtOAc and washed with water and brine and the crude material was purified using an ISCO Combiflash unit (MeOH in DCM: 0-1%) to obtain the title product as a solid. (27 mg, 50% yield). 1H NMR (400 MHz, CD3OD) δ=3.17 (s, 3H), 4.02 (s, 3H), 4.44 (s, 2H), 7.27 (d, J=8.8 Hz, 1H), 7.94 (d, J=8.8 Hz, 1H). MS (ES+): m/z 223.19 (100) [MH+]; HPLC: tR=0.76 min (UPLC, analytical).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399433B2
Source datasetuspto-grants-2013_03
ORD IDord-90663d918e084cac90d3edd9d7a229d7
Source noteuspto-grants-2013_03