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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022895Generated: October 27, 2026

1,2-Dibromoethane → Methyl 5-bromo-3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylate

https://huagongshe.com/reaction/1022895

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantDiisopropylamineHCID 7912—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylateHCID 2805185—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 5-bromo-3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylateHCID 56965789—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of diisopropylamine (20 mL) in tetrahydrofuran (200 mL) was added 1.6M n-butyllithium/hexane solution (82.4 mL) while stirring under ice-cooling, and the mixture was stirred at 0° C. for 15 min. After stirring, the reaction system was cooled to −78° C., and a solution of methyl 3-[(trifluoroacetyl)amino]thiophene-2-carboxylate (10 g) in tetrahydrofuran (50 mL) was added dropwise. After the completion of the dropwise addition, the mixture was stirred at the same temperature for 1 hr, and 1,2-dibromoethane (20.6 mL) was added. After stirring at the same temperature for 30 min, the reaction system was allowed to warm to room temperature, and further stirred for 30 min. The reaction system was poured into saturated aqueous sodium hydrogen carbonate (600 mL), and the mixture was extracted with ethyl acetate, washed with brine, and dried over anhydrous sodium sulfate. Insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (5.3 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722660B2
Source datasetuspto-grants-2014_05
ORD IDord-a943cabd0a5c4a819c743f6218c4f7ab
Source noteuspto-grants-2014_05