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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106826Generated: October 31, 2026

N-bromobutanimide → Ethyl 2-bromomethyl-4-(3-nitrophenyl)-6-phenyl-3-pyridinecarboxylate

https://huagongshe.com/reaction/2106826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 2-methyl-4-(3-nitrophenyl)-6-phenyl-3-pyridinecarboxylateHCID 10248079—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 2-bromomethyl-4-(3-nitrophenyl)-6-phenyl-3-pyridinecarboxylateHCID 1038856132.8%

Reaction Steps

A mixture of ethyl 2-methyl-4-(3-nitrophenyl)-6-phenyl-3-pyridinecarboxylate (5 g), N-bromosuccinimide (5.9 g) and benzoyl peroxide (0.1 g) in carbon tetrachloride (200 ml) was refluxed for 5 hours. The reaction mixture was poured into ice water (100 ml). The separated organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride successively, dried over magnesium sulfate and evaporated in vacuo. The residue was subjected to a column chromatography on silica gel eluting with a mixture of n-hexane and chloroform (1:2 V/V). The fractions containing the desired compound were combined and evaporated in vacuo to give ethyl 2-bromomethyl-4-(3-nitrophenyl)-6-phenyl-3-pyridinecarboxylate (2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931453
Source datasetuspto-grants-1990_06
ORD IDord-d6367dc0f0c24c40a0cadf52168483e1
Source noteuspto-grants-1990_06