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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394865Generated: October 28, 2026

Methyl iodide → HCID 18630315, compound

https://huagongshe.com/reaction/2394865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 18630229HCID 18630229—
SolventDimethylformamideHCID 6228—
ProductHCID 18630315HCID 1863031596%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of N-ethyl-N-methyl 2-(N-tert-butylamino)benzamide (1.89 g, 8.1 mmol), potassium carbonate (2.2 g, 15.9 mmol), and methyl iodide (2.3 g, 16.2 mmol) in DMF (40 mL) was heated overnight at 40° C., then was partitioned between EtOAc and water. The EtOAc was dried (MgSO4), concentrated, and purified by HPLC with 1:4 ethyl acetate/cyclohexane to afford 1.923 g of N-ethyl-N-methyl 2-(N-methyl-N-tert-butylamino)benzamide as a yellow oil, a 96% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811411
Source datasetuspto-grants-1998_09
ORD IDord-fcb89e2b806640259c34dc193f8ee79b
Source noteuspto-grants-1998_09