Basic information Safety Supplier Related

2-chloro-4-nitrobenzyl alcohol

Basic information Safety Supplier Related

2-chloro-4-nitrobenzyl alcohol Basic information

Product Name:
2-chloro-4-nitrobenzyl alcohol
Synonyms:
  • 2-chloro-4-nitrobenzyl alcohol
  • 2-Chloro-4-nitrobenzenemethanol
  • Einecs 257-828-2
  • Benzenemethanol, 2-chloro-4-nitro-
CAS:
52301-88-9
MF:
C7H6ClNO3
MW:
187.58
EINECS:
257-828-2
Mol File:
52301-88-9.mol
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2-chloro-4-nitrobenzyl alcohol Chemical Properties

Melting point:
83 °C
Boiling point:
337.0±27.0 °C(Predicted)
Density 
1.476±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
13.20±0.10(Predicted)
Appearance
Light yellow to brown Solid
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Safety Information

HS Code 
2906290090
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2-chloro-4-nitrobenzyl alcohol Usage And Synthesis

Synthesis

13324-11-3

52301-88-9

General procedure for the synthesis of 2-chloro-4-nitrobenzyl alcohol from methyl 2-chloro-4-nitrobenzoate: In a 250 mL round-bottom flask, methyl 2-chloro-4-nitrobenzoate (5 g, 23 mmol) was dissolved in anhydrous dichloromethane (100 mL). The reaction system was cooled to -78 °C under nitrogen protection. Bis(2-methylpropyl)alumina (35 mL, 35 mmol, 1 M solution in hexane) was added slowly and dropwise. The reaction mixture was kept stirred at -78 °C for 4 h. The reaction was subsequently quenched by the addition of water (5 mL). The reaction mixture was gradually warmed to room temperature over 20 min. Anhydrous sodium sulfate (15 g) was added to dry it. after 10 min, the desiccant was removed by filtration. The filtrate was concentrated under reduced pressure to give 2-chloro-4-nitrobenzyl alcohol in 95% yield.

References

[1] Patent: WO2010/132999, 2010, A1. Location in patent: Page/Page column 91

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