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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | 1-Amino-1-methylurea | HCID 256004 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-[(E)-(4-bromophenyl)methylideneamino]-1-methylurea | HCID 117727902 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193736B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-362d1fac14ff47369da0d3dcde69de63 |
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| Source note | uspto-grants-2015_11 |
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