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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219818Generated: November 2, 2026

Methyl iodide → HCID 87782457, compound

https://huagongshe.com/reaction/2219818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 46919612HCID 46919612—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87782457HCID 8778245710.4%

Reaction Steps

To a stirred solution of 5-{4-[(1E)-N-hydroxy-2,2-dimethylpropanimidoyl]-phenyl}-1-methyl-1H-pyrrole-2-carbonitrile (0.212 g, 0.75 mmol) in THF (7 mL) was added sodium hydride (0.03 g, 60% in mineral oil, 0.75 mmol) at 0° C. After the mixture was stirred for 10 minutes, methyl iodide (0.8 mL, 1.28 mmol) was added and the resulting mixture was stirred overnight at room temperature. The reaction mixture was then quenched with a saturated ammonium chloride solution (20 mL), and extracted several times with ethyl acetate (3×20 mL). The combined organic layers were dried over magnesium sulfate and concentrated. The residue was purified by a silica gel column (5% ethyl acetate in hexane) to afford 5-{4-[(1E)-N-methoxy-2,2-dimethylpropanimidoyl]phenyl}-1-methyl-1H-pyrrole-2-carbonitrile as a white solid (0.023 g, 10%). MS (ES) m/z 296.0; HRMS: calcd for C18H21N3O+H+, 296.17574; found (ESI, [M+H]+), 296.1753.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414142B2
Source datasetuspto-grants-2008_08
ORD IDord-87b376b1be8043e9b762986be0dec48a
Source noteuspto-grants-2008_08