HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923235Generated: October 25, 2026
Acetic Anhydride → 2,5-Dimethoxy-4-methylbenzonitrile
https://huagongshe.com/reaction/923235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 2,5-Dimethoxy-4-methylbenzaldehyde | HCID 602019 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2,5-Dimethoxy-4-methylbenzonitrile | HCID 595738 | — |
Reaction Steps
By analogy to steps outlined in J. Med. Chem. 1976, 19(12), 1400-1404. 2,5-dimethoxy-4-methylbenzaldehyde (14.8 g, 82.2 mmol) is dissolved in pyridine (300 mL) and to it, is added hydroxylamine hydrochloride (6.8 g, 98.6 mmol). The suspension is heated at 105° C. for 2 h. Acetic anhydride (15.5 mL, 164 mmol) is then added to the reaction and stirring is continued for another 2 h. The solution is evaporated to dryness and partitioned between EtOAc and saturated aqueous NaHCO3. The organic fraction is dried (Na2SO4) and evaporated to give a yellow solid which is taken up in hexanes and filtered to give 2,5-dimethoxy-4-methylbenzonitrile as a white solid. (cas #51267-09-5) MS (ESI) m/z 178.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278969B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-7707d99c93584beb8e030dfa8499c61d |
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| Source note | uspto-grants-2016_03 |
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