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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzonitrile, 4-bromo- | HCID 12162 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Bromo-N'-hydroxybenzene-1-carboximidamide | HCID 2756838 | 84.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415482B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-3a6f27639a944d6f898938c65c4a7fb1 |
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| Source note | uspto-grants-2013_04 |
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