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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558612Generated: October 31, 2026

N-bromobutanimide → HCID 67000967, compound

https://huagongshe.com/reaction/558612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 20099814HCID 20099814—
SolventAcetonitrileHCID 6342—
ProductHCID 67000967HCID 6700096772.9%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of 5-(4-trifluoromethyl-phenyl)-pyridin-2-ylamine (example C.25 step 1) (3.9 g, 16 mmol) in acetonitrile (65 mL) at 0° C. was added NBS (2.914 g, 16 mmol) and the mixture was stirred at 23° C. for 2 h. Poured on ice with sat. NaHCO3-sol., extracted thrice with AcOEt, dried the combined organic layers over Na2SO4, filtered off and evaporated. The residue was purified by silica gel column chromatography with AcOEt followed by trituration with heptane and very little ether to give the title compound as a light brown solid (3.7 g, 71%). MS (ISP) 317 [(M+H)+], 319 [(M+2+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063048B2
Source datasetuspto-grants-2011_11
ORD IDord-e28bd1b298be444cb4d486959dc4f6ae
Source noteuspto-grants-2011_11