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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727340Generated: October 25, 2026

Hydrogen Bromide → Benzene, 1-bromo-3-ethyl-

https://huagongshe.com/reaction/1727340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant3-EthylanilineHCID 11475—
ReactantSodium NitriteHCID 23668193—
Catalystcopper(I) bromideHCID 24593—
SolventHydroxy(oxo)-lambda4-sulfaneHCID 5326661—
ProductBenzene, 1-bromo-3-ethyl-HCID 12317040%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-ethylaniline (10.0 g, 82.5 mmol) in 50% sulfanic acid (43.6 g) was added dropwise an aqueous solution (16.5 mL) of sodium nitrite (6.83 g, 99.0 mmol) over 30 minutes at 0° C. The resulting reaction mixture was stirred for 45 minutes at 0° C. This diazonium salt solution was added dropwise to a solution of copper (I) bromide (12.4 g, 86.6 mmol) in a 48% hydrobromic acid (82.5 mL) while heating gently under reflux. After the addition, the reaction mixture was heated to reflux for 30 minutes. The reaction mixture was cooled to room temperature, and extracted with ether. The extracts were sequentially washed with a 1N-aqueous sodium hydroxide solution and brine, and filtrated, dried, and concentrated. The residue was purified by silica gel column chromatography (hexane-ethyl acetate=20:1) to obtain a title compound (6.13 g, yield 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495018B2
Source datasetuspto-grants-2009_02
ORD IDord-ea2e14a1de50471bb3fdb50fa2708a93
Source noteuspto-grants-2009_02