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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162583Generated: October 26, 2026

N-bromobutanimide → Ethyl 6-(bromomethyl)picolinate

https://huagongshe.com/reaction/1162583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 6-methylpyridine-2-carboxylateHCID 564597—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 6-(bromomethyl)picolinateHCID 2303375598.3%

Reaction Steps

A mixture of 6-methyl-pyridine-2-carboxylic acid ethyl ester (1.65 g, 10 mmol), NBS (1.77 g, 10 mmol), and benzoyl peroxide (100 mg) in carbon tetrachloride (20 ml) was refluxed for 14 h. After cooling to room temperature, the reaction mixture was partitioned between diethyl ether and water (120 ml, 4:1), organic layer was washed with water (2×20 ml), brine, dried (MgSO4), filtered and concentrated to give 6-bromomethyl-pyridine-2-carboxylic acid ethyl ester (2.4 g) which was used without further purification. LCMS m/z: 245 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820704B2
Source datasetuspto-grants-2010_10
ORD IDord-68468710087740078ac5874558b61ab5
Source noteuspto-grants-2010_10