Difference between revisions of "Oxalyl chloride"

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| Solubility = Reacts
 
| Solubility = Reacts
| SolubleOther = Reacts with alcohols
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| SolubleOther = Reacts with alcohols, amines, [[carboxylic acid]]s
 
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===Chemical===
 
===Chemical===
 
Oxalyl chloride behaves similarly to other [[acyl chloride]]s in that reacting with alcohols produces the corresponding [[ester]]. Unusually, however, reaction with water does not yield the parent acid, but instead results in decomposition to [[carbon dioxide]], [[carbon monoxide]], and [[hydrogen chloride]].
 
Oxalyl chloride behaves similarly to other [[acyl chloride]]s in that reacting with alcohols produces the corresponding [[ester]]. Unusually, however, reaction with water does not yield the parent acid, but instead results in decomposition to [[carbon dioxide]], [[carbon monoxide]], and [[hydrogen chloride]].
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: C<sub>2</sub>O<sub>2</sub>Cl<sub>2</sub> + H<sub>2</sub>O → 2 HCl + CO<sub>2</sub> + CO
  
 
Other [[carboxylic acid]]s can be converted to the corresponding acyl chloride by treatment with oxalyl chloride in the presence of a catalytic amount of a nitrogen base such as [[dimethylformamide]], [[triethylamine]], or [[pyridine]]. The byproducts produced by this reaction are [[carbon dioxide]] and [[carbon monoxide]].
 
Other [[carboxylic acid]]s can be converted to the corresponding acyl chloride by treatment with oxalyl chloride in the presence of a catalytic amount of a nitrogen base such as [[dimethylformamide]], [[triethylamine]], or [[pyridine]]. The byproducts produced by this reaction are [[carbon dioxide]] and [[carbon monoxide]].
  
Oxalyl chloride can also be used to formylate [[arene]]s by [[Friedel-Crafts acylation]].
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Oxalyl chloride can also be used to formylate [[arene]]s by [[Friedel-Crafts_reaction#Friedel-Crafts_acylation|Friedel-Crafts acylation]].
  
 
===Physical===
 
===Physical===
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==Preparation==
 
==Preparation==
Oxalyl chloride is prepared by reacting [[anhydrous]] [[oxalic acid]] with [[phosphorus pentachloride]].
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Oxalyl chloride is usually prepared by reacting [[anhydrous]] [[oxalic acid]] with [[phosphorus pentachloride]]. Unusually, [[thionyl chloride]] cannot be used to chlorinate oxalic acid.
  
 
==Projects==
 
==Projects==
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==Handling==
 
==Handling==
 
 
===Safety===
 
===Safety===
 
Oxalyl chloride is very toxic and presents a severe inhalational hazard. It should only be used with very good ventilation.
 
Oxalyl chloride is very toxic and presents a severe inhalational hazard. It should only be used with very good ventilation.
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===Storage===
 
===Storage===
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In airtight bottles.
  
 
===Disposal===
 
===Disposal===
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Should be dissolved in an excess calcium hydroxide solution, which will cause calcium oxalate to precipitate.
  
 
==References==
 
==References==
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[[Category:Irritants]]
 
[[Category:Irritants]]
 
[[Category:Chlorinating agents]]
 
[[Category:Chlorinating agents]]
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[[Category:Liquids]]

Latest revision as of 21:47, 11 October 2022

Oxalyl chloride
Names
IUPAC name
Oxalyl dichloride
Systematic IUPAC name
Ethanedioyl dichloride
Other names
Oxalic acid chloride
Oxalic acid dichloride
Oxalic dichloride
Oxaloyl chloride
Properties
C2O2Cl2
Molar mass 126.93 g/mol
Appearance Colorless liquid
Odor Acrid
Density 1.4785 g/cm3
Melting point −16 °C (3 °F; 257 K)
Boiling point 63–64 °C (145–147 °F; 336–337 K)
Reacts
Solubility Reacts with alcohols, amines, carboxylic acids
Hazards
Safety data sheet Sigma-Aldrich
Flash point Non-flammable
Related compounds
Related compounds
Oxalic acid
Thionyl chloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Oxalyl chloride is the acyl chloride of oxalic acid. It is used as a chlorinating agent, similar to thionyl chloride. Like other acyl chlorides, it is also used for producing derivatives of the parent acid such as esters. Aromatic esters of oxalic acid are used in glowsticks.

Properties

Chemical

Oxalyl chloride behaves similarly to other acyl chlorides in that reacting with alcohols produces the corresponding ester. Unusually, however, reaction with water does not yield the parent acid, but instead results in decomposition to carbon dioxide, carbon monoxide, and hydrogen chloride.

C2O2Cl2 + H2O → 2 HCl + CO2 + CO

Other carboxylic acids can be converted to the corresponding acyl chloride by treatment with oxalyl chloride in the presence of a catalytic amount of a nitrogen base such as dimethylformamide, triethylamine, or pyridine. The byproducts produced by this reaction are carbon dioxide and carbon monoxide.

Oxalyl chloride can also be used to formylate arenes by Friedel-Crafts acylation.

Physical

Availability

Oxalyl chloride is available from chemical suppliers but due to its hazards it is often hard to get for amateurs.

Preparation

Oxalyl chloride is usually prepared by reacting anhydrous oxalic acid with phosphorus pentachloride. Unusually, thionyl chloride cannot be used to chlorinate oxalic acid.

Projects

  • Make Bis(2,4,6-trichlorophenyl)oxalate for glowsticks

Handling

Safety

Oxalyl chloride is very toxic and presents a severe inhalational hazard. It should only be used with very good ventilation.

Contact with water produces highly toxic carbon monoxide gas, along with corrosive hydrogen chloride.

Storage

In airtight bottles.

Disposal

Should be dissolved in an excess calcium hydroxide solution, which will cause calcium oxalate to precipitate.

References

Relevant Sciencemadness threads