HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438240Generated: October 31, 2026
4-Bromo-2-methylbenzoic acid → (4-Bromo-2-methylphenyl)methanol
https://huagongshe.com/reaction/1438240
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromo-2-methylbenzoic acid | HCID 99570 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Bromo-2-methylphenyl)methanol | HCID 22280088 | 90% |
Reaction Steps
4-Bromo-2-methyl-benzoic acid (9.88 g, 45.9 mmol) was dissolved in THF (100 ml), and the solution was cooled to 0° C. To this solution, a solution of 1M BH3.THF (91.89 ml, 91.89 mmol) was added at 0° C., and the solution was vigorously stirred for 3 hours at room temperature. The reaction mixture was diluted with cold water (20 mL), washed with a saturated solution of NaHCO3, then extracted with ether 3 times (300 mL). The combined organic ether was washed with brine (250 mL), dried over MgSO4, and concentrated in Vacuo. The residue was purified via flash column chromatography (25% to 55% EtOAc in Hexane) to give white solid (8.24 g, 90% yield). 1H NMR (400 MHz, CDCl3) δ: 2.32 (2H, s) 4.64 (1H, d, J=5.81 Hz) 7.20-7.26 (2H, m) 7.30-7.36 (1H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07622605B2 |
|---|
| Source dataset | uspto-grants-2009_11 |
|---|
| ORD ID | ord-416c3c90ecfc4aa3911dcbd73f778a1b |
|---|
| Source note | uspto-grants-2009_11 |
|---|