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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439708Generated: October 27, 2026

Methyl iodide → HCID 22402970, compound

https://huagongshe.com/reaction/439708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178497326HCID 178497326—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22402970HCID 22402970—

Reaction Steps

Sodium methoxide (1.98 g, 36.6 mmol) is added to a solution of dimethyl 2-methyl-4,5-benzimidazoledicarboxylate (7.44 g, 33.3 mmol) in methanol and tetrahydrofuran. After 5 minutes, iodomethane (2.18 mL, 35.0 mmol) is added and the mixture is stirred for 24 hours at room temperature. Additional sodium methoxide (1.80 g, 33.3 mmol) and iodomethane (2.07 mL, 33.3 mmol) are added and stirring is continued for another 15 hours. The reaction mixture is concentrated in vacuo to give a residue which is dispersed in dilute hydrochloric acid, and treated with sodium bicarbonate to pH 8 and extracted with chloroform. The combined organic extracts are dried (MgSO4) and concentrated in vacuo to give a residue which is recrystallized from ethyl acetate to afford the title product as an orange solid, mp 205°-208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05516751
Source datasetuspto-grants-1996_05
ORD IDord-cc8c380d1628433f97609dc10b11f248
Source noteuspto-grants-1996_05