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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836797Generated: October 26, 2026

Hydrogen Peroxide → 3-Bromo-6-methoxybenzene-1,2-diol

https://huagongshe.com/reaction/1836797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant6-Bromo-2-hydroxy-3-methoxybenzaldehydeHCID 262237—
SolventSodium HydroxideHCID 14798—
Product3-Bromo-6-methoxybenzene-1,2-diolHCID 370587464.2%

Reaction Steps

Aldehyde 12 (23 g) was suspended in 2% sodium hydroxide (300 mL) and a solution of 30% hydrogen peroxide (15.8 g, 1.4 eq.) was added. After 2 hours, another portion of 30% hydrogen peroxide (1.4 eq.) was added and the solution stirred overnight. The reaction mixture was acidified, extracted with dichloromethane, washed with sodium thiosulfate and the solvent removed in vacuo to afford a tan solid. The solid was recrystallized from methanol to afford colorless crystals (14 g, 64%): m.p. 122.3-124.3° C., lit20 m.p. 124-126° C.; EIMS m/z 220 (M+, 81Br), 218 (M+, 79Br), 205, 203, 177, 175, 95; 1HNMR δ 6.99 (1H, d, J=9.0 Hz, H5), 6.42 (1H, d, J=9.0 Hz, H4), 5.56 (1H, s, OH), 5.51 (1H, s, OH), 3.88 (3H, s, OCH3); 13C—NMR (75.5 MHZ) δ 146.59, 140.95, 133.47, 122.21, 104.35, 101.55, 56.31; Anal. Calcd. For C7H7O3Br: C, 38.39; H, 3.22. Found: C, 38.47; H, 3.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777578B2
Source datasetuspto-grants-2004_08
ORD IDord-b1548f03209b4fb5bb7bd38971776b78
Source noteuspto-grants-2004_08