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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641467Generated: October 27, 2026

Dimethylformamide → 5-chloro-N-(1-cyclopropylethyl)-2-nitrobenzamide

https://huagongshe.com/reaction/1641467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant5-Chloro-2-nitrobenzoic acidHCID 17286—
ReactantThionyl ChlorideHCID 24386—
Reactant1-CyclopropylethanamineHCID 519239—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product5-chloro-N-(1-cyclopropylethyl)-2-nitrobenzamideHCID 4339944675%

Reaction Steps

A mixed liquid comprising 25 g of 5-chloro-2-nitrobenzic acid, 25 ml of toluene, 22.2 g of thionyl chloride and 0.1 ml of dimethylformamide was refluxed with heating for 1 hour to prepare acid chloride. 18.0 g of triethylamine was added to a mixed solution comprising 13.75 g of 1-cyclopropylethylamine and 375 ml of tetrahydrofuran and cooled with ice. The above prepared acid chloride was dissolved in 30 ml of toluene and dropwise added under cooling with ice. After completion of dropwise addition, reaction was carried out at room temperature for 15 hours. After completion of the reaction, the reaction mixture was poured to water, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution and dried over sodium sulfate, and ethyl acetate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 25 g of the pale yellow desired product (melting point: 137 to 141° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08115006B2
Source datasetuspto-grants-2012_02
ORD IDord-44b97b7faad1420f99652d583aba81f3
Source noteuspto-grants-2012_02