HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2086522Erstellt: 25. Oktober 2026
5-Bromosalicylic acid → 4-Hydroxy[1,1'-biphenyl]-3-carboxylic acid
https://huagongshe.com/reaction/2086522
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 5-Bromosalicylic acid | HCID 6972 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Phenyl dihydrogen orthoborate | HCID 78412 | — |
| Edukt | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-Hydroxy[1,1'-biphenyl]-3-carboxylic acid | HCID 67584 | 89,2% |
Reaktionsschritte
In 400 ml of water, 21.7 g of 5-bromosalicylic acid, 13.41 g of phenylboric acid and 15.28 g of potassium carbonate were dissolved. The solution was stirred at room temperature for 40 minutes. After the completion of the reaction was confirmed with TLC, the reaction liquid was poured into a mixed medium of diluted hydrochloric acidethyl acetate. The mixture was extracted, and the organic phase was collected and washed with saturated sodium chloride aqueous solution. After dried with magnesium sulfate, the liquid was concentrated to form a crude product. The product was recrystallized from acetonitrile to obtain 18.58 g of 5-phenylsalicylic acid in the form of colorless crystallites. The yield was 87%. The product was confirmed with NMR and mass spectroscopy.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06726966B2 |
|---|
| Quelldatensatz | uspto-grants-2004_04 |
|---|
| ORD ID | ord-e14dc147047b414ba7fc96fbc80376d9 |
|---|
| Quellennotiz | uspto-grants-2004_04 |
|---|