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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264198Generated: November 1, 2026

Water → [4-[(4-Bromo-2-methylphenyl)ethylamino]-2-chlorophenyl](2-methylphenyl)methanone

https://huagongshe.com/reaction/1264198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantHCID 10180060HCID 10180060—
SolventTetrahydrofuranHCID 8028—
Product[4-[(4-Bromo-2-methylphenyl)ethylamino]-2-chlorophenyl](2-methylphenyl)methanoneHCID 10275183—

Reaction Steps

A solution of 4-(4-bromo-2-methyl-phenylamino)-2-chloro-2′-methylbenzophenone (Compound 136)(110 mg) in dry tetrahydrofurane (2.0 ml was added sodium hydride (19 mg) in one portion under stirring. After 10 min at room temperature ethyl iodide (124 mg ) was added and the reaction mixture was stirred for 18 hours under reflux, then poured into water and extracted with EtOAc. The organic phases were separated, dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by chromatography using a mixture of EtOAc/pentane 1:8 as eluant to yield the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541670B2
Source datasetuspto-grants-2003_04
ORD IDord-829ca5a29def435d88ac3fb44dac5dbf
Source noteuspto-grants-2003_04