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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718644Generated: October 26, 2026

Acetic Acid → 1-[(E)-(4-bromophenyl)methylideneamino]-1-methylurea

https://huagongshe.com/reaction/718644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
Reactant4-BromobenzaldehydeHCID 70741—
Reactant1-Amino-1-methylureaHCID 256004—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product1-[(E)-(4-bromophenyl)methylideneamino]-1-methylureaHCID 117727902—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-bromobenzaldehyde (4.3 g, 23 mmol) and 1-amino-1-methylurea (2.5 g, 28 mmol) in EtOH (40 mL) was added AcOH (2.5 mL) and water (4.5 mL). The resulting solution was stirred overnight at 80° C. and allowed to cool to rt. A precipitate formed by the addition of Et2O (50 mL). The solids were collected by filtration and compound 51a was obtained as a white solid. Mass Spectrum (LCMS, ESI pos.): Calcd. for C9H10BrN3O: 256.0 (M+H). Found 256.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193736B2
Source datasetuspto-grants-2015_11
ORD IDord-362d1fac14ff47369da0d3dcde69de63
Source noteuspto-grants-2015_11