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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554522Generated: October 26, 2026

Water → (2-Benzyloxyphenyl)-(3-fluorophenyl)methanol

https://huagongshe.com/reaction/554522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-FluorobenzaldehydeHCID 68009—
Reactant1-(Benzyloxy)-2-bromobenzeneHCID 561828—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product(2-Benzyloxyphenyl)-(3-fluorophenyl)methanolHCID 4996332065%

Reaction Steps

In a nitrogen stream, an n-butyllithium hexane solution (2.44 M, 5.65 mL) was added dropwise to a solution of 1-benzyloxy-2-bromobenzene (3.3 g, 12.5 mmol) in THF (40 mL) at −78° C. and the mixture solution was stirred at the same temperature for 30 minutes. To this mixture, a solution of 3-fluorobenzaldehyde (1.40 g, 11.3 mmol) in THF (5 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 (1:10)] to obtain the title compound (2.26 g, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048897B2
Source datasetuspto-grants-2011_11
ORD IDord-7bded00815184a5381800886c1709187
Source noteuspto-grants-2011_11