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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259711Generated: October 31, 2026

Benzyl Bromide → HCID 22402944, compound

https://huagongshe.com/reaction/259711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178497326HCID 178497326—
SolventDimethylformamideHCID 6228—
ProductHCID 22402944HCID 2240294445.8%

Reaction Steps

Sodium hydride (0.750 g, 80% oil dispersion, 25.0 mmol) is added, in portions, to a solution of dimethyl 2-methyl-4,5-benzimidazoledicarboxylate (6.07 g, 24.6 mmol) in dry dimethylformamide at 0° C. with stirring. After evolution of hydrogen ceases, benzyl bromide (2.93 mL, 24.6 mmol) is added to the reaction mixture and stirring is continued for 16 hours. The reaction mixture is concentrated in vacuo and the resultant residue is dispersed in methylene chloride and water. The phases are separated and the aqueous phase is extracted with methylene chloride. The organic phases are combined, dried and concentrated in vacuo to afford a solid residue. Recrystallization of the solid from ethyl acetate affords the title product as an off-white powder (3.81 g, 45.0%), mp 192°-195° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523279
Source datasetuspto-grants-1996_06
ORD IDord-6064342c0f1d4f7a984c027912ee1b4d
Source noteuspto-grants-1996_06