HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264749Generated: October 26, 2026
Acetic Anhydride → 5-Bromo-2-methoxybenzonitrile
https://huagongshe.com/reaction/264749
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Bromo-2-methoxybenzaldehyde | HCID 90684 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Bromo-2-methoxybenzonitrile | HCID 4418560 | — |
Reaction Steps
A mixture of 5-Bromo-o-anisaldehyde (6.45 g), hydroxylamine hydrochloride (2.2 g), sodium acetate (4.1 g) and acetic acid (20 mL) was heated at 100 ° C. with stirring for 1 h. Acetic anhydride was added (20 mL) and the mixture was refluxed for 8 h. The reaction mixture was poured onto ice water and the mixture was made basic by the careful addition of 50% sodium hydroxide. The product was extracted with ether, the ether extracts were dried over magnesium sulfate and the sovent was removed in vacuo. The residue was crystallized from ether/hexane to afford 5-Bromo-2-methoxy-benzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646280 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-b6043656dfe24c09833bc4f307bc72ed |
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| Source note | uspto-grants-1997_07 |
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