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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913841Generated: October 31, 2026

Sulfuric Acid → HCID 5251666, compound

https://huagongshe.com/reaction/1913841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant1,4-DibromobenzeneHCID 7804—
ReactantSodium HydroxideHCID 14798—
ReactantSodiumHCID 5360545—
SolventWaterHCID 962—
ProductHCID 5251666HCID 525166686%

Reaction Conditions

Temperature150 °C

Reaction Steps

A modification of the published procedures of H. Borns, Annalen der Chemie 1877, 187, 350 was used. A 300 mL round-bottom flask equipped with a reflux condenser, stirring bar, and gas inlet was charged with 1,4-dibromobenzene (118 g, 0.50 moles) and 30% fuming sulfuric acid (76 mL). The mixture was heated to 150° C. for 3 hours under nitrogen to give a clear solution. The solution was cooled to room temperature to give a solidified mass and transferred into a beaker with water to give a slurry. The slurry was treated with 50% sodium hydroxide solution (130 g) and diluted to 900 mL with water with heating to disperse the precipitated solids. The mixture was cooled to room temperature and the solids collected by vacuum filtration under a rubber dam. The solids were washed with two times with isopropanol (200 mL) and air dried on the filter then dried under vacuum at 100° C. to give 159 g (93% crude yield). The product was recrystallized from ethanol/water (4:1) and dried under vacuum at 150° C. to give 146 g (86% yield) of 2,5-dibromobenzenesulfonic acid, sodium salt. 1H NMR (DMSO-d6): 7.42 (dd, 8.4, 2.6 Hz, 1H), 7.53 (d, 8.4 Hz, 1H), 8.01 (d, 2.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609804B2
Source datasetuspto-grants-2013_12
ORD IDord-c4bea2143741479f96f63509db846064
Source noteuspto-grants-2013_12