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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554546Generated: October 30, 2026

Ethyl Acetate → 2-Benzyloxy-6-methoxybenzyl alcohol

https://huagongshe.com/reaction/554546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium Sodium TartrateHCID 9357—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant2-Benzyloxy-6-methyl-benzoic acid ethyl esterHCID 67461909—
SolventDiethyl EtherHCID 3283—
Product2-Benzyloxy-6-methoxybenzyl alcoholHCID 67458610100%

Reaction Steps

In a nitrogen stream, to a suspension of lithium aluminum hydride (0.82 g, 21.50 mmol) in ether (30 mL), a solution of 2-benzyloxy-6-methyl-benzoic acid ethyl ester (4.47 g, 16.54 mmol) in ether (15 mL) was added at room temperature over 10 minutes. The reaction mixture was stirred under heating to reflux for one hour. Ethyl acetate (2 mL) was added dropwise to the reaction mixture under cooling with ice, and then a saturated Rochelle salt aqueous solution (20 mL) was added thereto dropwise and the mixture was stirred at room temperature for one hour. The reaction mixture was subjected to Celite filtration. To the filtrate was added a saturated Rochelle salt aqueous solution (10 mL) and the mixture was extracted with ether. The organic layer was washed with a saturated sodium chloride aqueous solution and dried (anhydrous sodium sulfate), and then the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:4)] to obtain the title compound (3.84 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048897B2
Source datasetuspto-grants-2011_11
ORD IDord-132d322bef7844dd9ae14ec044f8800b
Source noteuspto-grants-2011_11