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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966414Generated: October 25, 2026

Hydrochloric Acid → 3,5-Diethyl-1-bromobenzene

https://huagongshe.com/reaction/966414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Bromo-2,6-diethylanilineHCID 611452—
ReactantPhosphinic AcidHCID 4124402—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3,5-Diethyl-1-bromobenzeneHCID 1195902996.3%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A mixture of 20 g of 4-bromo-2,6-diethylaniline, 160 ml of acetic acid, 100 ml of concentrated HCl solution, 30 ml of water and 100 ml of EtOH is cooled to −5° C., a solution of 6.6 g of sodium nitrite in 25 ml of water is added dropwise and the mixture is left stirring at RT for 30 minutes. The reaction mixture is poured into 170 ml of 50% H3PO2 cooled to 0° C. and is left stirring for 2 hours at 0° C. and then for 48 hours at RT. The reaction mixture is extracted with ether, the organic phase is washed with water, with 1N NaOH solution, with water and dried over Na2SO4, and the solvent is evaporated off under vacuum. The residue is chromatographed on silica gel, eluting with cyclohexane. 18 g of the expected product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951940B2
Source datasetuspto-grants-2005_10
ORD IDord-667f37d09fe947118a531078c60814f6
Source noteuspto-grants-2005_10