Acetone cyanohydrin
Skeletal formula of acetone cyanohydrin
Ball and stick model of acetone cyanohydrin
Ball and stick model of acetone cyanohydrin
Spacefill model of acetone cyanohydrin
Spacefill model of acetone cyanohydrin
Names
Preferred IUPAC name
2-Hydroxy-2-methylpropanenitrile[1]
Other names
  • Cyanohydrin-2-propanone[2]
  • α-Hydroxyisobutyronitrile[2]
  • 2-Hydroxy-2-methyl-propionitrile[2]
Identifiers
3D model (JSmol)
3DMet
605391
ChEBI
ChemSpider
DrugBank
ECHA InfoCard 100.000.828
EC Number
  • 200-909-4
KEGG
MeSH acetone+cyanohydrin
RTECS number
  • OD9275000
UNII
UN number 1541
  • InChI=1S/C4H7NO/c1-4(2,6)3-5/h6H,1-2H3 checkY
    Key: MWFMGBPGAXYFAR-UHFFFAOYSA-N checkY
  • CC(C)(O)C#N
Properties
C4H7NO
Molar mass 85.106 g·mol−1
Appearance Colourless liquid
Density 932 mg·mL−1
Melting point −21.2 °C; −6.3 °F; 251.9 K
Boiling point 95 °C; 203 °F; 368 K
Vapor pressure 2 kPa (at 20 °C)
1.399
Thermochemistry
−121.7 to −120.1 kJ·mol−1
−2.4514 to −2.4498 MJ·mol−1
Hazards
GHS labelling:
GHS06: Toxic GHS09: Environmental hazard
Danger
H300, H310, H330, H410
P260, P273, P280, P284, P301+P310
NFPA 704 (fire diamond)
NFPA 704 four-colored diamond
4
1
2
Flash point 75 °C (167 °F; 348 K)
Explosive limits 2.25–11%
Lethal dose or concentration (LD, LC):
  • 15.8 mg·kg−1 (dermal, rabbit)
  • 18.65 mg·kg−1 (oral, rat)
NIOSH (US health exposure limits):
PEL (Permissible)
 None[2]
REL (Recommended)
 C 1 ppm (4 mg·m−3) [15-minute][2]
IDLH (Immediate danger)
 N.D.[2]
Safety data sheet (SDS) fishersci.com
Related compounds
Related alkanenitriles
Related compounds
 DBNPA
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Acetone cyanohydrin (ACH) is an organic compound used in the production of methyl methacrylate, the monomer of the transparent plastic polymethyl methacrylate (PMMA), also known as acrylic. It liberates hydrogen cyanide easily, so it is used as a source of such. For this reason, this cyanohydrin is also highly toxic.

Preparation

In the laboratory, this compound may be prepared by treating sodium cyanide with acetone, followed by acidification:[3]

Considering the high toxicity of acetone cyanohydrin, a lab scale production has been developed using a microreactor-scale flow chemistry[4] to avoid needing to manufacture and store large quantities of the reagent. Alternatively, a simplified procedure involves the action of sodium or potassium cyanide on the sodium bisulfite adduct of acetone prepared in situ. This gives a less pure product, one that is nonetheless suitable for most syntheses.[5]

Reactions

Acetone cyanohydrin is an intermediate en route to methyl methacrylate.[6] Treatment with sulfuric acid gives the sulfate ester of the methacrylamide, methanolysis of which gives ammonium bisulfate and methyl methacrylate.[7]

It is used as a surrogate in place of HCN, as illustrated by its use as a precursor to lithium cyanide:[8]

(CH3)2C(OH)CN + LiH → (CH3)2CO + LiCN + H2

In transhydrocyanation, an equivalent of HCN is transferred from acetone cyanohydrin to another acceptor, with acetone as byproduct. The transfer is an equilibrium process, initiated by base. The reaction can be driven by trapping reactions or by the use of a superior HCN acceptor, such as an aldehyde.[9] In the hydrocyanation reaction of butadiene, the transfer is irreversible.[10]

Natural occurrence

Cassava tubers contain linamarin, a glucoside of acetohydrin, and the enzyme linamarase for hydrolysing the glucoside. Crushing the tubers releases these compounds and produces acetone cyanohydrin.

Safety

Acetone cyanohydrin is classified as an extremely hazardous substance in the US Emergency Planning and Community Right-to-Know Act and carries an RCRA P069 waste code. The principal hazards of acetone cyanohydrin arise from its ready decomposition on contact with water, which releases highly toxic hydrogen cyanide.

References

  1. ↑ "acetone cyanohydrin - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 16 September 2004. Identification. Retrieved 8 June 2012.
  2. 1 2 3 4 5 6 NIOSH Pocket Guide to Chemical Hazards. "#0005". National Institute for Occupational Safety and Health (NIOSH).
  3. ↑ Cox, R. F. B.; Stormont, R. T. "Acetone Cyanohydrin". Organic Syntheses.; Collective Volume, vol. 2, p. 7
  4. ↑ Heugebaert, Thomas S. A.; Roman, Bart I.; De Blieck, Ann; Stevens, Christian V. (2010-08-11). "A safe production method for acetone cyanohydrin". Tetrahedron Letters. 51 (32): 4189–4191. doi:10.1016/j.tetlet.2010.06.004.
  5. ↑ Wagner, E. C.; Baizer, Manuel. "5,5-Dimethylhydantoin". Organic Syntheses.; Collective Volume, vol. 3, p. 323
  6. ↑ Wiley, Richard H.; Waddey, Walter E. (1949). "Methacrylamide". Organic Syntheses. 29: 61. doi:10.15227/orgsyn.029.0061.
  7. ↑ Bauer, William, Jr. "Methacrylic Acid and Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a16_441. ISBN 978-3527306732.{{cite encyclopedia}}: CS1 maint: multiple names: authors list (link).
  8. ↑ Tom Livinghouse (1981). "Trimethylsilyl Cyanide: Cyanosilylation of p-Benzoquinone". Org. Synth. 60: 126. doi:10.15227/orgsyn.060.0126.
  9. ↑ Haroutounian, Serkos A. (2001). "Acetone Cyanohydrin". Encyclopedia of Reagents for Organic Synthesis. eEROS. doi:10.1002/047084289X.ra014. ISBN 0471936235.
  10. ↑ Bini, L.; Müller, C.; Wilting, J.; von Chrzanowski, L.; Spek, A. L.; Vogt, D. (October 2007). "Highly selective hydrocyanation of butadiene toward 3-pentenenitrile". J. Am. Chem. Soc. 129 (42): 12622–12623. doi:10.1021/ja074922e. hdl:1874/26892. PMID 17902667.
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