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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554498Generated: October 26, 2026

Cuminaldehyde → (2-Benzyloxyphenyl)-(4-isopropylphenyl)methanol

https://huagongshe.com/reaction/554498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCuminaldehydeHCID 326—
ReactantWaterHCID 962—
Reactant1-(Benzyloxy)-2-bromobenzeneHCID 561828—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product(2-Benzyloxyphenyl)-(4-isopropylphenyl)methanolHCID 6745962084%

Reaction Steps

In a nitrogen stream, an n-butyllithium hexane solution (2.44 M, 5.14 mL) was added dropwise to a solution of 1-benzyloxy-2-bromobenzene (3.0 g, 11.4 mmol) in THF (114 mL) at −78° C. and the reaction mixture was stirred at the same temperature for 30 minutes. To this solution, a solution of 4-isopropylbenzaldehyde (1.41 g, 9.49 mmol) in THF (38 mL) was added dropwise at −78° C. The reaction mixture was stirred at the same temperature for one hour and furthermore at 0° C. for one hour. 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 (2.63 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048897B2
Source datasetuspto-grants-2011_11
ORD IDord-f2976ad2a9a04cc49d3278293327f678
Source noteuspto-grants-2011_11