HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Acetylbenzoic Acid → 4-(2-Amino-1,3-thiazol-4-yl)benzoic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Acetylbenzoic Acid | HCID 11470 | — |
| Edukt | Bromine | HCID 24408 | — |
| Edukt | Carbonyl bromide | HCID 79057 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Edukt | Thiourea | HCID 2723790 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-(2-Amino-1,3-thiazol-4-yl)benzoic acid | HCID 613179 | — |
Reaktionsschritte
A solution of 4-acetyl-benzoic acid (10 g, 61 mmol), in HOAc (400 mL) at 55° C. was treated with bromine (1 eq., 3.12 mL) dropwise over 10 minutes. After 90 minutes the reaction was cooled, the acetic acid was removed, ethyl acetate (50 mL) was added and then removed to get rid of the remainder of the acetic acid. The crude bromo ketone was then dissolved in ethanol (200 mL) with NaOAc (12 g) and thiourea (1 eq. 4.4 g) was added. The suspension was stirred at room temperature for 15 hours. The solvents were removed and the solids washed with water (3×100 mL) then ether:ethanol (4:1, 3×100 mL) and dried to give the product as a tan solid. MS: 221.2 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07595398B2 |
| Quelldatensatz | uspto-grants-2009_09 |
| ORD ID | ord-d29e033db8d04bd3b35694af9be5cf39 |
| Quellennotiz | uspto-grants-2009_09 |