N-(3-nitrophenyl)propionamide

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N-(3-nitrophenyl)propionamide Basic information
Product Name:N-(3-nitrophenyl)propionamide
Synonyms:N-(3-nitrophenyl)propionamide;Propanamide, N-(3-nitrophenyl)-
CAS:7470-50-0
MF:C9H10N2O3
MW:194.19
EINECS:231-267-3
Product Categories:
Mol File:7470-50-0.mol
N-(3-nitrophenyl)propionamide Structure
N-(3-nitrophenyl)propionamide Chemical Properties
Melting point 104-104.5 °C
Boiling point 384.9±25.0 °C(Predicted)
density 1.287±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka14.20±0.70(Predicted)
Safety Information
MSDS Information
N-(3-nitrophenyl)propionamide Usage And Synthesis
Synthesis
Propionyl chloride

79-03-8

3-Nitroaniline

99-09-2

N-(3-nitrophenyl)propionamide

7470-50-0

3-Nitroaniline (1.2 g, 8.7 mmol) was dissolved in anhydrous dichloromethane (50 mL) and triethylamine (6 mL, 43.0 mmol) was added. Propionyl chloride (1.5 mL, 17 mmol) was slowly added dropwise under ice bath conditions, and stirring was continued in the ice bath after the drop was completed. Subsequently, the reaction mixture was allowed to slowly warm up to room temperature and stirring was continued for 2 hours. Upon completion of the reaction, the reaction mixture was diluted with water (150 mL) and then extracted with dichloromethane (150 mL x 3). The organic phases were combined, dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure to remove the solvent. The crude product was purified by column chromatography (eluent: petroleum ether/ethyl acetate, v/v=3/1) to afford 1.6 g of the light yellow solid product N-(3-nitrophenyl)propionamide in 95% yield.

References[1] Patent: CN106432246, 2017, A. Location in patent: Paragraph 0453; 0602; 0603; 0604; 0605
N-(3-nitrophenyl)propionamide Preparation Products And Raw materials
Raw materialsPropionyl chloride-->3-Nitroaniline-->Triethylamine-->Dichloromethane
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