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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116587Generated: October 31, 2026

Methyl iodide → HCID 22139640, compound

https://huagongshe.com/reaction/2116587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAcetic AnhydrideHCID 7918—
Reactant4-PyridinemethanamineHCID 77317—
SolventMethanolHCID 887—
ProductHCID 22139640HCID 2213964070.7%

Reaction Steps

To a cold (ice-water bath) solution of 4-picolylamine (1070 gr, 9.9 mol) in methanol (3 l) was added dropwise acetic anhydride (1400 gr, 13.7 mol). During addition the reaction temperature was kept between 10 and 30° C. When the addition of the reagent was complete the reaction mixture was left overnight at room temperature. Iodomethane (800 ml, 24.8 mol) was added to the reaction mixture which was cooled with water bath, under nitrogen atmosphere. During addition the reaction temperature was kept below 25° C. When the addition was complete, the reaction mixture was protected from light and left at room temperature overnight The excess iodomethane was evaporated, crystallization was induced, the reaction mixture was cooled (ice bath) and isopropanol (1.5 l) was added. The reaction mixture was left at −30° C. overnight, the precipitate was filtered off, washed with isopropanol and dried. 4-(Acetaminomethyl)-1-methyl-pyridinium iodide (2043 gr, 7 mol) was obtained as yellow powder (71% yield). 1H-NMR (D2O) δ 2.10 (s, CH3CO), 4.32 (s, CH3N+), 4.63 (s, CH2NHCO), 7.89 (d, j=6.6 Hz, 2H), 8.67 (d, j=6.6 Hz, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439251B2
Source datasetuspto-grants-2008_10
ORD IDord-ca82a778b30346b69102abe4da54eaf0
Source noteuspto-grants-2008_10