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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223344Generated: October 30, 2026

Ethyl bromoacetate → HCID 13059431, compound

https://huagongshe.com/reaction/223344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantHCID 13059430HCID 13059430—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13059431HCID 1305943154%

Reaction Steps

A solution of methyl 4-(1H-imidazol-1-yl)-β-oxobenzenepropanoate (6.1 g, 0.025 mol) in tetrahydrofuran (65 ml) is added slowly to a stirred suspension of 50% NaH (1.2 g, 0.025 mol) in tetrahydrofuran (20 ml) and the solution is stirred for one additional hour. Ethyl bromoacetate (4.5 g) is added followed by refluxing the mixture for 7 to 8 hours. The tetrahydrofuran is removed, the residue is treated with water, and the organic material is extracted with ether. The residue obtained after removal of ether is hydrolysed by heating with 6 N HCl for 7 to 8 hours. The crude acid is finally crystallized from dimethylformamide to yield 3.3 g of the product 4-(1H-imidazol-1-yl)-γ-oxobenzenebutanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04353905
Source datasetuspto-grants-1982_10
ORD IDord-8c1af3a66af94737afaa498744771152
Source noteuspto-grants-1982_10