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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393166Generated: October 29, 2026

N-bromobutanimide → HCID 22648744, compound

https://huagongshe.com/reaction/393166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22648740HCID 22648740—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 22648744HCID 2264874489%

Reaction Steps

49.2 g (0.30 mol) of 1-(4-ethylpyrimidin-5-yl)propan-1-one was dissolved in 500 ml of carbon tetrachloride, and 53 g (0.30 mol) of N-bromosuccinimide and 0.3 g of azoisobutyronitrile were added, followed by refluxing for 2 hours. After cooling, crystals were removed by filtration, and the filtrate was concentrated and the obtained oily product was purified by column chromatography (ethyl acetate:n-hexane=1:4 to 1:2) to obtain 64.3 g (yield: 89%) of 2-bromo-1-(4-ethylpyrimidin-5-yl)-propan-1-one as yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806230B1
Source datasetuspto-grants-2004_10
ORD IDord-2af2835edd13433ab88fad3f2b6631b3
Source noteuspto-grants-2004_10