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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797304Generated: October 26, 2026

Hydrogen Bromide → [4-({4-Bromo-2-[(2-hydroxyethoxy)methyl]phenyl}amino)-2-chlorophenyl](2-methylphenyl)methanone

https://huagongshe.com/reaction/1797304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium HydroxideHCID 14798—
Reactant[2-Chloro-4-({2-[(hydroxyethoxy)methyl]phenyl}amino)phenyl](2-methylphenyl)methanoneHCID 10294143—
SolventDimethyl SulfoxideHCID 679—
Product[4-({4-Bromo-2-[(2-hydroxyethoxy)methyl]phenyl}amino)-2-chlorophenyl](2-methylphenyl)methanoneHCID 10227340—

Reaction Steps

Compound 156 (3.8 g, 9.6 mmol) was dissolved in DMSO (115 mL). The solution was cooled on an ice bath and 48% aqueous HBr (32 mL, 285 mmol) was added slowly. The solution was stirred in a closed vessel at room temperature for 5 days. The reaction mixture was cooled on an ice bath and 27% aqueous NaOH (30 mL) was added to give a basic solution. The water phase was extracted three times with EtOAc, the combined organic phases were washed with brine, dried (MgSO4), filtered and evaporated in vacuo. The crude product was purified by flash chromatography using EtOAc/petroleum ether 1:1 as the eluent to afford the title compound as a slightly coloured crystalline compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034015B2
Source datasetuspto-grants-2006_04
ORD IDord-00e0f76388c34fc7be24405c40a4aa4b
Source noteuspto-grants-2006_04