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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34286Generated: October 29, 2026

Catechol → 1,2-Bis(benzyloxy)benzene

https://huagongshe.com/reaction/34286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCatecholHCID 289—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product1,2-Bis(benzyloxy)benzeneHCID 124709593%

Reaction Steps

A mixture of catechol (11.0 g, 0.10M), benzylbromide (25.0 ml, 0.21M) and finely powdered anhydrous K2CO3 (44.2 g, 0.32M) in DMF (60 ml) was stirred at room temperature under N2 for 72 hours. The mixture was then diluted with Et2O and filtered. The ether solution was washed with three portions of distilled water, one portion of saturated NaCl solution, dried (K2CO3) and concentrated in vacuo. The residue was recrystallized from hexane to give dibenzyloxybenzene (27.04 g, 93% yield) as white crystals, mp 58°-59° C. (literature: Page et al., J. Org. Chem. 27, 218 (1962), mp 58°-59° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04761413
Source datasetuspto-grants-1988_08
ORD IDord-23dc90a19b1f4e4b84a75ac2f1b55b95
Source noteuspto-grants-1988_08