HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 714189Erstellt: 24. Oktober 2026
Acetone → 4-[3-Methoxy-4-(methoxymethoxy)phenyl]but-3-en-2-one
https://huagongshe.com/de/reaction/714189
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetone | HCID 180 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 3-Methoxy-4-(methoxymethoxy)benzaldehyde | HCID 79661 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-[3-Methoxy-4-(methoxymethoxy)phenyl]but-3-en-2-one | HCID 69501682 | 97,7% |
Reaktionsschritte
4-Methoxymethyloxy-3-methoxybenzaldehyde (1j, 2.30 g, 11.7 mmol) and acetone (19, 8.75 ml, 118.4 mmol) were combined in ethanol (20 ml) and stirred for 15 min at room temperature. A solution of sodium hydroxide (0.80 g, 20.0 mmol) and water (20 ml) was added and the mixture stirred for 1 hr at room temperature. The resulting mixture was extracted into ethyl acetate, washed with saturated sodium chloride, dried over magnesium sulfate, filtered and evaporated to afford a solid. The crude solid was recrystallized from hexane to give 2.70 g (97%) of a white solid: mp 73-75° C.; 1H NMR: δ 2.34 (s, 3H), 3.48 (s, 3H), 3.89 (s, 3H), 5.24 (s, 2H), 6.58 (d, 1H, J=16.1 Hz), 7.07 (m, 2H), 7.13 (d, 1H, J=8.7 Hz), 7.43 (d, 1H, J=16.1 Hz); 13C NMR: δ 27.4, 55.9, 56.3, 95.2, 110.4, 115.9, 122.5, 125.7, 128.7, 143.1, 148.7, 149.8, 198.0.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09187397B2 |
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| Quelldatensatz | uspto-grants-2015_11 |
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| ORD ID | ord-738f3df2774248cd809c7e3afb861164 |
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| Quellennotiz | uspto-grants-2015_11 |
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