HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triisopropyl borate → 2,3-Difluoro4-(4-pentyloxybutoxy)phenylboronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1,2-Difluoro-3-(4-pentyloxybutoxy)benzene | HCID 22016262 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,3-Difluoro4-(4-pentyloxybutoxy)phenylboronic acid | HCID 22016255 | — |
Reaction Steps
To a solution of 1,2-difluoro-3-(4-pentyloxybutoxy)-benzene (24), (1 equi.) in THF (5 mL/mmole), butyllithium (1.3 equi.) was added at −78° C. The reaction mixture was stirred at that temperature for 2 h,. Then triisopropylborate (1 equi.) was added at that temperature. The reaction mixture was stirred at that temperature for 1 h and at room temperature for 10 h, quenched with water, extracted with ethyl acetate, washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by recrystallization from hexane gave 2,3-difluoro-4-(4-pentyloxybutoxy)phenylboronic acid (25), as a white solid (75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07083832B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-3e1233a3cb904efd828fd79e64ba9c58 |
| Source note | uspto-grants-2006_08 |