HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883622Generated: November 2, 2026
Acetic Acid → (5-Bromo-2-methylphenyl)methanol
https://huagongshe.com/reaction/1883622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 5-Bromo-2-methylbenzaldehyde | HCID 10420289 | — |
| Reactant | HCID 178418435 | HCID 178418435 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | (5-Bromo-2-methylphenyl)methanol | HCID 12993770 | 103.2% |
Reaction Steps
161.2 g (810 mmol) of 5-bromo-2-methylbenzaldehyde was dissolved in 1.5 L of tetrahydrofuran and 150 ml of water, and to the resulted solution was dropped, at 15 to 20° C., a solution prepared by dissolving 10.0 g (264 mmol) of sodium boron hydride in 100 ml of a 0.1 wt % sodium hydroxide aqueous solution. After completion of dropping, the mixture was stirred at 15 to 20° C. for 4 hours. To the reaction solution was dropped 12.0 g of glacial acetic acid at 20° C. or lower, then, this was poured into ice water. The reaction solution was extracted with t-butyl methyl ether, the organic layer was washed with water, further washed twice with a saturated sodium bicarbonate solution, then, washed with saturated saline, and dried over anhydrous magnesium sulfate, then, concentrated to obtain 168 g of 5-bromo-2-methylbenzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06762197B2 |
|---|
| Source dataset | uspto-grants-2004_07 |
|---|
| ORD ID | ord-d540d75667754b1399a43f0c7522fa10 |
|---|
| Source note | uspto-grants-2004_07 |
|---|