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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195024Generated: November 2, 2026

Hydrogen Bromide → 2-Bromo-1,3-diethyl-5-methylbenzene

https://huagongshe.com/reaction/2195024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSulfamic AcidHCID 5987—
Reactant2,6-Diethyl-p-toluidineHCID 90536—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product2-Bromo-1,3-diethyl-5-methylbenzeneHCID 11579491—

Reaction Conditions

Temperature80 °C

Reaction Steps

To an initial charge of 65 ml of 48% aqueous HBr are added, in portions, 16.33 g [0.1 mol] of 2,6-diethyl-4-methylaniline. The resulting thick suspension is stirred at 80° C. for 15 minutes. It is then cooled to −10° C., and a solution of 8 g [0.116 mol] of NaNO2 in 35 ml of water is added dropwise within approx. 1 h at such a rate that the temperature does not exceed −5° C. 80 mg of sulphamic acid are added. Then the suspension of the diazonium salt, cooled to −10° C., is metered within about 30 minutes into a solution, heated to 80° C., of 13.9 g [0.05 mol] of FeSO4×7H2O in 65 ml of 62% aqueous HBr. The reaction mixture is then stirred at 80° C. for another 1 hour, allowed to cool to room temperature and admixed with 125 ml of water, the phases are separated and the aqueous phase is extracted three times with 50 ml each time of methylene chloride. The combined organic phases are washed twice with 25 ml each time of water, dried and concentrated under reduced pressure. This gives 21.3 g of an oil which, according to GC, contains 94.6% 2,6-diethyl-4-methylbromobenzene (89% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334417B2
Source datasetuspto-grants-2012_12
ORD IDord-2603e50ac02c4fba90782e972bd2e0a8
Source noteuspto-grants-2012_12