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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197120Generated: November 2, 2026

Pyridine → HCID 13961199, compound

https://huagongshe.com/reaction/1197120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromoacetyl bromideHCID 61147—
ReactantHCID 13961197HCID 13961197—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 13961199HCID 13961199—

Reaction Steps

20.9 g (0.66 mol) of ethyl 4-amino-3-(2-chlorobenzoyl)-phenylacetate are dissolved in 170 ml of anhydrous dioxane. First 5.2 ml of absolute pyridine are added and then 13.3 g (0.066 mol) of bromoacetylbromide are added dropwise at room temperature and the mixture is stirred for 24 hours. The suspension is filtered through Kieselgur. The Kieselgur is washed with ether, and the combined filtrates are concentrated in vacuo. The resulting residue is induced to crystallise by addition of ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116971
Source datasetuspto-grants-1992_05
ORD IDord-e1db2ca806d6460a88d9876bbab13ed4
Source noteuspto-grants-1992_05