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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant5-Bromo-2-methylbenzaldehydeHCID 10420289—
ReactantHCID 178418435HCID 178418435—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product(5-Bromo-2-methylphenyl)methanolHCID 12993770103.2%

Reaction Conditions

Temperature17.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762197B2
Source datasetuspto-grants-2004_07
ORD IDord-d540d75667754b1399a43f0c7522fa10
Source noteuspto-grants-2004_07