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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963975Generated: October 30, 2026

Benzonitrile, 4-bromo- → 4-Bromo-N'-hydroxybenzene-1-carboximidamide

https://huagongshe.com/reaction/1963975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrile, 4-bromo-HCID 12162—
ReactantDiisopropylethylamineHCID 81531—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventEthanolHCID 702—
Product4-Bromo-N'-hydroxybenzene-1-carboximidamideHCID 275683884.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 4-bromobenzonitrile (5.0 g, 27.5 mmol) in ethanol (42 ml) at room temperature, hydroxylamine hydrochloride (1.91 g, 27.5 mmol) and DIPEA (4.8 ml, 27.5 mmol) were added. The reaction mixture was stirred at 90° C. for 5 hours. After cooled to room temperature, the resulting mixture was concentrated to yield a colorless viscous liquid. The liquid was extracted with ethyl acetate and the organic layer was dried over magnesium sulfate, filtered and then concentrated to give a crude compound, which was washed with n-hexane to yield product 15 as a white solid (5.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415482B2
Source datasetuspto-grants-2013_04
ORD IDord-3a6f27639a944d6f898938c65c4a7fb1
Source noteuspto-grants-2013_04