HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 390649Erstellt: 25. Oktober 2026
Trimethyl borate → [3-(Methylamino)phenyl]boronic acid
https://huagongshe.com/reaction/390649
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trimethyl borate | HCID 8470 | — |
| Edukt | Benzenemethanamine, 3-bromo- | HCID 457587 | — |
| Edukt | HCID 178418306 | HCID 178418306 | — |
| Edukt | HCID 178418348 | HCID 178418348 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Pentane | HCID 8003 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | [3-(Methylamino)phenyl]boronic acid | HCID 23558980 | 40% |
Reaktionsschritte
161 mL (242 mmol) of 1.5M methyllithium in diethyl ether are added dropwise to a solution precooled to −78° C. of 37.6 g (202 mmol) of (3-bromophenyl)methylamine (prepared according to Example 24f) in 300 mL of tetrahydrofuran. After stirring for 1 hour at −78° C., 261 mL (444 mmol) of a 1.7M solution of tert-butyllithium in pentane are added dropwise and the medium is again stirred at −78° C. for 1 hour. At −65° C., 103.5 mL (808 mmol) of trimethyl borate are added dropwise and the reaction medium is then stirred, while allowing the temperature to rise to room temperature over 1 hour. After addition of ice, the reaction medium is extracted with a 1/1 heptane/ethyl acetate mixture and then with 1-butanol. The organic phases are combined, washed with water, dried over magnesium sulfate, filtered and evaporated; 11 g (40%) of 3-methylaminophenylboronic acid are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08383652B2 |
|---|
| Quelldatensatz | uspto-grants-2013_02 |
|---|
| ORD ID | ord-b428150b7c4f48f1a717c700223a4d6d |
|---|
| Quellennotiz | uspto-grants-2013_02 |
|---|