Basic information Safety Supplier Related

ALPHA-CHLORO-4-NITROBENZALDOXIME

Basic information Safety Supplier Related

ALPHA-CHLORO-4-NITROBENZALDOXIME Basic information

Product Name:
ALPHA-CHLORO-4-NITROBENZALDOXIME
Synonyms:
  • P-NITROBENZOHYDROXIMOYL CHLORIDE
  • a-Chloro-4-nitrobenzaldoxime
  • -Chloro-4-nitrobenzaldoxime
  • N-hydroxy-4-nitrobenziMidoyl chloride
  • Benzenecarboximidoyl chloride, N-hydroxy-4-nitro-
  • ALPHA-CHLORO-4-NITROBENZALDOXIME
  • 4-nitrobenzohydroximoyl chloride
CAS:
1011-84-3
MF:
C7H5ClN2O3
MW:
200.58
Mol File:
1011-84-3.mol
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ALPHA-CHLORO-4-NITROBENZALDOXIME Chemical Properties

Melting point:
66-67 °C
Boiling point:
376.6±44.0 °C(Predicted)
Density 
1.50±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
9.73±0.70(Predicted)
Appearance
Light yellow to yellow Solid
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ALPHA-CHLORO-4-NITROBENZALDOXIME Usage And Synthesis

Synthesis Reference(s)

The Journal of Organic Chemistry, 36, p. 2146, 1971 DOI: 10.1021/jo00814a024

Synthesis

1129-37-9

1011-84-3

General procedure for the synthesis of 4-nitrochlorobenzaldehyde oxime from 4-nitrobenzaldoxime: 4-nitrobenzaldoxime (087 mg, 5.3 mmol) was dissolved in anhydrous dimethylformamide (4.6 mL) and the solution was cooled down to 0 °C. N-chlorosuccinimide (800 mg, 6.0 mmol) was added in batches with stirring. The cooling bath was removed and the resulting mixture was stirred at room temperature for 4 hours. After completion of the reaction, ice water (20 mL) was added and the resulting mixture was extracted with ether. The organic layer was washed three times with water, once with saturated brine and dried with anhydrous magnesium sulfate. The solvent was removed under reduced pressure after filtration to give a white solid 4-nitrochlorobenzaldehyde oxime (1.064 g, 100%).1H NMR (400 MHz, CDCl3) data were as follows: δ 8.37 (s, 1H, -OH), 8.27 (d, J = 8.8 Hz, 2H, Ar-H), 8.04 (d, J = 8.8 Hz, 2H, Ar-H).

References

[1] Patent: WO2011/15037, 2011, A1. Location in patent: Page/Page column 42; 53
[2] Patent: US2011/212975, 2011, A1. Location in patent: Page/Page column 14; 19
[3] Tetrahedron Letters, 2006, vol. 47, # 9, p. 1457 - 1460
[4] Journal of Chemical Research, 2007, # 1, p. 26 - 28
[5] Tetrahedron, 2000, vol. 56, # 8, p. 1057 - 1064

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