Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398778Generated: October 31, 2026

2-Bromo-4-methylaniline → HCID 68764242, compound

https://huagongshe.com/reaction/1398778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-methylanilineHCID 11422—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantEthyl 4-[2,4-dichloro-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]butanoateHCID 68761768—
SolventO-XyleneHCID 7237—
ProductHCID 68764242HCID 6876424268%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of ethyl 4-[2,4-dichloro-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]butanoate (Reference Example 33; 1.50 g, 4.04 mmol), 2-bromo-4-methylaniline (1.0 mL, 8.08 mmol), p-toluenesulfonic acid monohydrate (822.2 mg, 4.32 mmol) and xylene (5.0 mL) was stirred at 130° C. for 12 hr. After cooling, the reaction mixture was neutralized with aqueous saturated sodium hydrogen carbonate and extracted with ethyl acetate (×3). The combined organic layer was washed with brine (×1), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with a 0-30% ethyl acetate/n-hexane gradient mixture to give the title compound as an oil (1.42 g, 2.73 mmol, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-2aed95d79a514b6c82f3cd99949abd8e
Source noteuspto-grants-2014_12