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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274600Generated: October 26, 2026

Formaldehyde → Methyl 4-[[2-ethyl-4-methyl-1H-imidazol-1-yl]methyl]benzoate

https://huagongshe.com/reaction/274600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantImidazoleHCID 795—
ReactantMethyl 4-(bromomethyl)benzoateHCID 256687—
ReactantSodium AcetateHCID 517045—
ReactantHCID 178437635HCID 178437635—
SolventAcetic AcidHCID 176—
ProductMethyl 4-[[2-ethyl-4-methyl-1H-imidazol-1-yl]methyl]benzoateHCID 20093489—

Reaction Steps

Methyl 4-[[2-ethyl-4-methyl-1H-imidazol-1-yl]methyl]benzoate compound was prepared from 2-ethyl-4-methyl-imidazole and (4-carbmethoxy) benzylbromide in an analogous fashion as described in Example 11. A solution of the above imidazole (2.17 g, 8.14 mmol), NaOAc (1.17 g), 37 % HCHO (10 mn) , and AcOH (1.2 mn) was heated under reflux for 22 hours. The solution was evaporated under vacuo, and the residue was stirred with 10 mL of 20% NaOH solution for 2 hours. It was diluted with water and the solution was extracted with CH2Cl2. The extract was washed with water, dried, and evaporated to an oil. It was chromatographed (CH2Cl2 /MeOH, 2-5%) to give 1.0 g of the desired hydroxymethyl compound as a foam. MS (CI 288 (m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389661
Source datasetuspto-grants-1995_02
ORD IDord-eb617010b0b044a0bf4beee044bbf93f
Source noteuspto-grants-1995_02