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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306192Generated: November 1, 2026

Triethylamine → 1-(triphenylmethyl)-1H-Imidazole-4-acetic acid methyl ester

https://huagongshe.com/reaction/2306192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromotriphenylmethaneHCID 11692—
ReactantHCID 178499561HCID 178499561—
SolventDimethylformamideHCID 6228—
Product1-(triphenylmethyl)-1H-Imidazole-4-acetic acid methyl esterHCID 10523967—

Reaction Steps

To a solution of methyl 4-imidazoleacetate hydrochloride, as described above in Step A, (4.30 g, 24.3 mmol) in dry DMF (50 mL) were added triethylamine (7.45 mL, 53.5 mmol), then triphenylmethyl bromide (8.64 g, 26.7 mmol). The mixture was stirred at ambient temperature for 18 hours, then partitioned between H2O (250 mL) and EtOAc (250 mL). The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica, eluting with EtOAc, to yield the product as a pale solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441017B1
Source datasetuspto-grants-2002_08
ORD IDord-797c492c52f74987a2af259a3cf321f9
Source noteuspto-grants-2002_08