Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phosphoric Acid | HCID 1004 | — |
| Edukt | Tributyl borate | HCID 12712 | — |
| Edukt | 6-Bromoindole | HCID 676493 | — |
| Edukt | HCID 178418306 | HCID 178418306 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 1H-Indol-6-ylboronic acid | HCID 2763205 | — |
Reaktionsschritte
A solution of 6-bromoindole (200 mg, 1.02 mmol) in anhydrous ether (4 mL), at −78° C., is treated dropwise with tert-butyllithium (1.7 M solution in pentane, 2 mL, 3.4 mmol). After stirring for 30 minutes the mixture is treated dropwise with tributyl borate (0.822 mL, 3.06 mmol) and allowed to warm up to room temperature. After stirring overnight the reaction mixture is diluted with ether, and this mixture is added in portions to phosphoric acid (15 mL, 1M), stirred for 30 minutes and extracted three times with ether (20 mL). The combined extracts are extracted three times with sodium hydroxide solution (20 mL, 1N). The combined sodium hydroxide extracts are acidified with phosphoric acid (1 M) to pH=2, extracted with ether. The combined ether extracts are washed with brine, dried over sodium sulfate and concentrated to obtain 1H-indol-6-yl-boronic acid [Intermediate (77)] as a solid, which is used for the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08193183B2 |
|---|
| Quelldatensatz | uspto-grants-2012_06 |
|---|
| ORD ID | ord-c59cc83136d0472ebf08a7048a01d54f |
|---|
| Quellennotiz | uspto-grants-2012_06 |
|---|