HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31959Erstellt: 24. Oktober 2026
Hydrochloric Acid → 4-(Diphenylamino)phenylboronic Acid (contains varying amounts of Anhydride)
https://huagongshe.com/de/reaction/31959
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Triisopropyl borate | HCID 21531 | — |
| Edukt | 4-Bromotriphenylamine | HCID 642838 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 4-(Diphenylamino)phenylboronic Acid (contains varying amounts of Anhydride) | HCID 12166934 | 70,6% |
Reaktionsschritte
A dry ethyl ether 100 ml and dry toluene 100 ml solution of 4-bromotriphenylamine 16.2 g was cooled down to −78° C. under argon atmosphere, and a hexane solution 32.8 ml of 1.6M normal butyllithium was dropwise added thereto. The reaction solution was stirred for one hour while heating up to 0° C. The reaction solution was cooled down again to −78° C., and a dry ether 50 ml solution of triisopropyl borate 23.5 g was dropwise added thereto. The reaction solution was stirred at room temperature for 5 hours. 1N hydrochloric acid 100 ml was added thereto and stirred for one hour, and then the aqueous layer was removed. The organic layer was dried on magnesium sulfate, and the solvent was distilled off. The solid matter thus obtained was washed with hexane and toluene to obtain 10.2 g of triphenylamine-4-boronic acid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07425654B2 |
|---|
| Quelldatensatz | uspto-grants-2008_09 |
|---|
| ORD ID | ord-24d318c5de6a4fe2b8dad79996897993 |
|---|
| Quellennotiz | uspto-grants-2008_09 |
|---|