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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605136Generated: October 26, 2026

Trifluoroacetic acid → 4-(4-Amino-phenoxy)-N-(4-bromo-phenyl)-3-nitro-benzamide

https://huagongshe.com/reaction/605136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant{4-[4-(4-Bromo-phenylcarbamoyl)-2-nitro-phenoxy]phenyl}-carbamic acid tert-butyl esterHCID 67040702—
SolventDichloromethaneHCID 6344—
Product4-(4-Amino-phenoxy)-N-(4-bromo-phenyl)-3-nitro-benzamideHCID 6704050697.2%

Reaction Steps

A solution of the product of Example 10B (250 mg, 0.4732 mmol) in methylene chloride (5 mL) was treated with trifluoroacetic acid (5 mL) at room temperature for 30 minutes. The solvents were removed by rotary evaporation under vacuum, and the residue taken up in ethyl acetate (100 mL) and washed with saturated aqueous sodium hydrogen carbonate (2×50 mL), water (50 mL), and brine (50 mL). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum to provide the title compound as a light orange solid (197 mg, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910595B2
Source datasetuspto-grants-2011_03
ORD IDord-ab2b9c3289ac4e2fa2c278a73a4f920c
Source noteuspto-grants-2011_03