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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554505Generated: October 25, 2026

Water → (2-Benzyloxyphenyl)-(4-methylsulfanyl-phenyl)methanol

https://huagongshe.com/reaction/554505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-(Methylthio)benzaldehydeHCID 76985—
Reactant1-(Benzyloxy)-2-bromobenzeneHCID 561828—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product(2-Benzyloxyphenyl)-(4-methylsulfanyl-phenyl)methanolHCID 6745972858%

Reaction Steps

In a nitrogen stream, an n-butyllithium hexane solution (1.59 M, 6.92 mL) was added dropwise to a solution of 1-benzyloxy-2-bromobenzene (2.89 g, 11.0 mmol) in THF (38 mL) at −78° C. and the mixture solution was stirred at the same temperature for 30 minutes. To this solution, a solution of 4-methylsulfanylbenzaldehyde (1.67 g, 11.0 mmol) in THF (12 mL) was added dropwise at −78° C. The reaction mixture was stirred at the same temperature for one hour, and then water was added thereto and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution and dried (anhydrous magnesium 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 (1:5)] to obtain the title compound (2.14 g, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048897B2
Source datasetuspto-grants-2011_11
ORD IDord-becdbd9e16964f3abdd2d43f65bd4051
Source noteuspto-grants-2011_11