HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1885070Erstellt: 26. Oktober 2026
Mesitylene → Benzenemethanol, 3,5-dimethyl-, 1-acetate
https://huagongshe.com/reaction/1885070
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Mesitylene | HCID 7947 | — |
| Edukt | N-Hydroxyphthalimide | HCID 10665 | — |
| Edukt | Tert-Butyl nitrite | HCID 10906 | — |
| Edukt | Benzaldehyde, 3,5-dimethyl- | HCID 34225 | — |
| Edukt | 3,5-Dimethylbenzonitrile | HCID 89718 | — |
| Edukt | N-[(3,5-Dimethylphenyl)methylidene]hydroxylamine | HCID 71401900 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | Benzenemethanol, 3,5-dimethyl-, 1-acetate | HCID 12229212 | — |
Reaktionsschritte
Mesitylene (1 ml), t-butyl nitrite (1 mmol), N-hydroxyphthalimide (0.2 mmol), and acetic acid (1 ml) were placed in a flask and were stirred at 60° C. in an atmosphere of argon gas (1 atm=0.101 MPa) for 20 hours. The resulting reaction mixture was analyzed to find that 3,5-dimethylbenzaldehyde oxime, 3,5-dimethylbenzaldehyde, 3,5-dimethylbenzonitrile, and 3,5-dimethylphenylmethyl acetate were formed in yields of 61%, 3%, 4%, and less than 1%, respectively.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06768023B2 |
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| Quelldatensatz | uspto-grants-2004_07 |
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| ORD ID | ord-6dbe78615a4b4b198597b09087a4073c |
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| Quellennotiz | uspto-grants-2004_07 |
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