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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976214Generated: November 1, 2026

Pyrogallol → 4-(3,5-Dimethoxy-benzyloxy)-2-ethoxy-benzo[1,3]dioxole

https://huagongshe.com/reaction/1976214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrogallolHCID 1057—
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
Reactant2-Ethoxy-benzo[1,3]dioxol-4-olHCID 13447063—
Reactant1-(Bromomethyl)-2,4-dimethoxybenzeneHCID 15151907—
SolventAcetoneHCID 180—
Product4-(3,5-Dimethoxy-benzyloxy)-2-ethoxy-benzo[1,3]dioxoleHCID 22000665—

Reaction Steps

2-Ethoxy-benzo[1,3]dioxol-4-ol (1.11 g, 6.08 mmol), 4-bromomethyl-1,3-dimethoxybenzene (1.17 g, 5.08 mmol), potassium carbonate (0.77 g, 5.59 mmol) and 18-crown-6-ether (0.13 g, 0.51 mmol) were stirred together at room temperature in acetone (40 cm3, 99%) under nitrogen for 18 hours. The solution was evaporated under reduced pressure, and the residue was taken up in dichloromethane (30 cm3) and water (30 cm3). The aqueous layer was extracted with dichloromethane (3×30 cm3), and the combined extracts were washed with water (2×50 cm3), dried (MgSO4), and evaporated under reduced pressure. The residue was chromatographed (SiO2, dichloromethane) to give the di protected pyrogallol, (1.56 g, 92%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225352B1
Source datasetuspto-grants-2001_05
ORD IDord-644d4b1f7098443785983ae2a6c8536d
Source noteuspto-grants-2001_05