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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494393Generated: October 26, 2026

Trifluoroacetic acid → Methyl (3-bromo-4-nitrophenyl)acetate

https://huagongshe.com/reaction/494393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(3-Bromo-4-nitrophenyl)malonic acid tert-butyl ester methyl esterHCID 57683269—
SolventChloroformHCID 6212—
ProductMethyl (3-bromo-4-nitrophenyl)acetateHCID 2351230494.9%

Reaction Steps

The 2-(3-bromo-4-nitrophenyl)malonic acid tert-butyl ester methyl ester (1.18 g) obtained in Example 4 a) was dissolved in chloroform (10 mL), trifluoroacetic acid (10 g) was added thereto under ice-cooling, and the mixture was stirred at room temperature for 5 hours. The reaction mixture was poured gradually into ice and saturated aqueous sodium bicarbonate, and extracted with ethyl acetate. The extract was washed with water and saturated brine, dried over sodium sulfate and concentrated to give the title compound (0.820 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538140B2
Source datasetuspto-grants-2009_05
ORD IDord-add141723c084d18b251c5a51095c2a1
Source noteuspto-grants-2009_05