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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604745Generated: October 30, 2026

1-Bromo-4-ethylbenzene → α-(4-Ethylphenyl)-2-(phenylmethoxy)benzenemethanol

https://huagongshe.com/reaction/604745

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-ethylbenzeneHCID 15313—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(Benzyloxy)benzaldehydeHCID 344784—
ReactantMagnesiumHCID 5462224—
Catalyst1-Bromo-4-ethylbenzeneHCID 15313—
SolventTetrahydrofuranHCID 8028—
Productα-(4-Ethylphenyl)-2-(phenylmethoxy)benzenemethanolHCID 67069123101.4%

Reaction Steps

1-Bromo-4-ethylbenzene (6.69 g, 0.036 mol) was added to a suspension of magnesium (17.2 g) and tetrahydrofuran (50 mL) and heated to reflux. Subsequently, a tetrahydrofuran (300 mL) solution of 1-bromo-4-ethylbenzene (97.9 g, 0.529 mol) was added for two hours at room temperature. After stirred at room temperature for 1.5 hours, the reaction mixture was cooled to 4° C. and a tetrahydrofuran (100 mL) solution of 2-benzyloxybenzaldehyde (100 g, 0.471 mol) was added for one hour. After stirred for two hours, the reaction mixture was poured into a saturated ammonium chloride aqueous solution. After the mixture was extracted with ethyl acetate, the organic phase was washed with brine and then dried with anhydrous magnesium sulfate. After the desiccant was filtered off, the residue obtained by evaporating the solvent under reduced pressure was purified by silica gel column chromatography (hexane:ethyl acetate=95:5) to obtain (2-benzyloxyphenyl)(4-ethylphenyl)methanol (152 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910619B2
Source datasetuspto-grants-2011_03
ORD IDord-504a6e10b67a44f99bff5e160191ec8b
Source noteuspto-grants-2011_03