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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914781Generated: October 25, 2026

Hydroquinone → 2-Bromo-1,4-benzenediol

https://huagongshe.com/reaction/1914781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantBromineHCID 24408—
ReactantChloroform methanolHCID 21584188—
Solventtert-Butyl methyl etherHCID 15413—
Product2-Bromo-1,4-benzenediolHCID 68502—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of hydroquinone Q-1 (10 g, 90.90 mmol) in MTBE (methyl tert-butyl ether) (100 mL) at −5° C. was added bromine (17.4 g, 90.90 mmol). The reaction mixture was stirred at 0° C. for 30 min. Solvent was removed in vacuo and the crude product was purified by column chromatography (SiO2, 2% MeOH—CHCl3) to afford compound Q-2 (13 g, 75%) as a solid. TLC Rf=0.6 (CHCl3-MeOH, 9:1); 1H NMR (CDCl3) δ 6.94 (app d, 1H), 6.88 (d, J=8.7 Hz, 1H), 6.72 (dd, J=8.7, 2.8 Hz, 1H), 5.19 (s, 2H) (Synlett 2000, 11, 1561-1564).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614237B2
Source datasetuspto-grants-2013_12
ORD IDord-0ccd451e670042eaa2c5e5a153cc8d9f
Source noteuspto-grants-2013_12