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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057755Generated: November 2, 2026

N-bromobutanimide → HCID 20330252, compound

https://huagongshe.com/reaction/2057755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 20330256HCID 20330256—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 20330252HCID 20330252—

Reaction Steps

A mixture of 10.5 g (0.046 mole) of 1-(5-chloro-2-pyridinyloxy)-3,3-dimethyl-2-butanone, prepared above, and 8.37 g (0.047 mole) N-bromosuccinimide (NBS) in 300 ml. carbon tetrachloride, with stirring, was irradiated and heated with a sunlamp until all of the NBS was consumed (about 45 min.). The reaction mixture was cooled, filtered, and the filtrate washed with aqueous sodium bisulfite and dried. After removal of the solvent, there was obtained a quantitative yield of 1-bromo-1-(5-chloro-2-pyridinyl-oxy)-3,3-dimethyl-2-butanone, a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04212869
Source datasetuspto-grants-1980_07
ORD IDord-fae2b7151896405191bcce88354888c3
Source noteuspto-grants-1980_07