HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538945Generated: October 31, 2026
Methyl 4-bromo-3-methylbenzoate → (4-Bromo-3-methylphenyl)methanol
https://huagongshe.com/reaction/538945
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-bromo-3-methylbenzoate | HCID 3294148 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Bromo-3-methylphenyl)methanol | HCID 10987288 | — |
Reaction Steps
A solution of methyl 4-bromo-3-methylbenzoate (2.0 g, 8.7 mmol) in dry THF (10 mL) was added to an ice-cooled suspension of lithium aluminiumhydride (400 mg, 10.4 mmol) in dry THF (30 mL). After addition, the mixture was warmed to room temperature and then stirred for 3 h. The excess lithium aluminiumhydride was quenched by successive addition of water (0.4 mL), 15% NaOHaq (0.4 mL), and water (1.2 mL) under ice cooling. The insoluble material appeared was removed by filtration (celite), and the precipitate was washed by AcOEt (20 mL×5). The combined filtrates were washed with brine (50 mL) and then dried over Na2SO4. The solvent was evaporated, and the obtained product (1.6 g, 100%) was used for next step without further purification. 1H-NMR (CDCl3, 400 MHz): δ7.53 (1H, d, J=8.1 Hz), 7.26 (1H, d, J=1.5 Hz), 6.40 (1H, dd, J=8.1, 1.5 Hz), 4.68 (2H, s), 2.44 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08865914B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-d85fdced7daa4f9c9d957852f869f8e5 |
|---|
| Source note | uspto-grants-2014_10 |
|---|