HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767621Generated: October 30, 2026
Hydrochloric Acid → 2-Methoxy-5-(trifluoromethyl)phenylboronic acid
https://huagongshe.com/reaction/1767621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1-Methoxy-4-(trifluoromethyl)benzene | HCID 600604 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methoxy-5-(trifluoromethyl)phenylboronic acid | HCID 2782676 | 81.8% |
Reaction Steps
A solution of 4-trifluoromethylanisole (8 g; 45 mmol) in dry THF (80 ml) at −30° C. under N2 was added a solution of 2.5 M n-BuLi in hexane (20 ml; 50 mmol). The reaction mixture was stirred for 1 h at −30° C., then cooled to −70° C. and added B(Oi-Pr)3 (14.1 ml; 64 mmol). The reaction mixture was allowed to slowly warm up to rt. over night. The reaction mixture was added 2 M HCl (40 ml) and THF was removed by evaporation. The aqueous remanense was extracted with Et2O (4×20 ml) and the combined organic fractions were extracted with 1 M NaOH (5×17 ml). The combined aqueous fractions were neutralized by 10 M HCl. The precipitate formed was isolated by filtration and washed with 1 M HCl to give 8.1 g (81%) product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07235548B2 |
|---|
| Source dataset | uspto-grants-2007_06 |
|---|
| ORD ID | ord-67183aac018141ab8ad6c4784413459a |
|---|
| Source note | uspto-grants-2007_06 |
|---|