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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172734Generated: November 2, 2026

4-Methoxybenzonitrile → HCID 178491258, compound

https://huagongshe.com/reaction/1172734

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzonitrileHCID 70129—
ReactantDiisopropylethylamineHCID 81531—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventEthanolHCID 702—
ProductHCID 178491258HCID 17849125898%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of 4-Methoxy-benzonitrile (1.07 g, 8 mmol) and DIEA (4.11 ml, 24 mmol) in EtOH (12.5 ml) was added 1.7 g of Hydroxylamine hydrochloride (24 mmol) and the reaction was heated at 70° C. for 48 h. Half of the solvent was removed under reduced pressure. The mixture was poured in DCM (100 ml) and water (30 ml). 2.5 ml of NaOH 1N was added until pH=9-10. The organic layer was separated and the aqueous phase was extracted with DCM. The organics layers were combined, washed with water, dried over MgSO4, filtered and evaporated under reduced pressure to afford 1.3 g (98%) of N-Hydroxy-4-methoxy-benzamidine as a colorless oil which can be used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834035B2
Source datasetuspto-grants-2010_11
ORD IDord-f4b395cca72a4b94929cab7aab22b651
Source noteuspto-grants-2010_11