HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1242893Erstellt: 23. Oktober 2026
Hydrochloric Acid → 4-[N-(4-Methoxybenzoyl)-N-methylamino]benzoic acid
https://huagongshe.com/de/reaction/1242893
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | p-Anisoyl chloride | HCID 7477 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 4-(Methylamino)benzoic acid | HCID 66345 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-[N-(4-Methoxybenzoyl)-N-methylamino]benzoic acid | HCID 21939734 | 51,3% |
Reaktionsschritte
Aqueous solution (50 ml) of sodium carbonate (23 g) was added to THF solution (50 ml) of 4-(methylamino)benzoic acid (5.0 g), and p-anisoyl chloride (5.6 g) was added dropwise to the solution under ice-cooling, which was stirred for 15 minutes, and then stirred at room temperature for 30 minutes. Concentrated hydrochloric acid was added to the reaction mixture under ice-cooling to make the water layer acidic, and extraction was conducted using ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride solution, dried, and then concentrated. The residue was purified using silica gel column chromatography (development solvent; hexane˜hexane:ethyl acetate=1:2), and recrystallized (ethyl acetate-hexane) to give the titled compound (4.8 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07115750B1 |
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| Quelldatensatz | uspto-grants-2006_10 |
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| ORD ID | ord-04ff0c0dc0be495995be898bf12ede25 |
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| Quellennotiz | uspto-grants-2006_10 |
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