Acetoacetanilide

Acetoacetanilide
Names
Preferred IUPAC name
3-Oxo-N-phenylbutanamide
Other names
Acetoacetylaminobenzene
Identifiers
CAS Number
  • 102-01-2 checkY
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL1604429
ChemSpider
  • 7311
ECHA InfoCard 100.002.725 Edit this at Wikidata
EC Number
  • 202-996-4
PubChem CID
  • 7592
UNII
  • W35JB9PY3X checkY
CompTox Dashboard (EPA)
  • DTXSID0024397 Edit this at Wikidata
InChI
  • InChI=1S/C10H11NO2/c1-8(12)7-10(13)11-9-5-3-2-4-6-9/h2-6H,7H2,1H3,(H,11,13)
    Key: DYRDKSSFIWVSNM-UHFFFAOYSA-N
  • InChI=1/C10H11NO2/c1-8(12)7-10(13)11-9-5-3-2-4-6-9/h2-6H,7H2,1H3,(H,11,13)
    Key: DYRDKSSFIWVSNM-UHFFFAOYAR
  • CC(=O)CC(=O)NC1=CC=CC=C1
Properties
Chemical formula
 C10H11NO2
Molar mass 177.203 g·mol−1
Appearance Colourless solid
Melting point 83 to 88 °C (181 to 190 °F; 356 to 361 K)
Solubility in water
 low
Hazards
GHS labelling:
Pictograms
 GHS07: Exclamation markGHS08: Health hazard
Warning
Hazard statements
 H302, H312, H332, H373
Precautionary statements
 P260, P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P314, P322, P330, P363, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
1
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Acetoacetanilide is an organic compound with the formula CH3C(O)CH2C(O)NHC6H5. It is the acetoacetamide derivative of aniline. It is a white solid that is poorly soluble in water. This chemical and many related compounds (prepared from various aniline derivatives) are used in the production of organic pigments called arylide yellows. Acetoacetanilides usually exist as the keto-amide tautomer according to X-ray crystallography.[1]

Preparation and reactions

Acetoacetanilide is prepared by acetoacetylation of aniline using diketene.[2] Many analogues have been prepared.[3]

To make the dyes, acetoacetanilides are coupled to diazonium salts, "azo coupling".[4]

Acetoacetylation with diketene followed by diazo coupling.

In the presence of sulfuric acid, acetoacetanilide dehydrates to give 4-methyl-2-quinolone.[5]

See also

  • C10H11NO2

References

  1. ^ Gilli, Paola; Bertolasi, Valerio; Ferretti, Valeria; Gilli, Gastone (2000). "Evidence for Intramolecular N−H···O Resonance-Assisted Hydrogen Bonding in β-Enaminones and Related Heterodienes. A Combined Crystal-Structural, IR and NMR Spectroscopic, and Quantum-Mechanical Investigation". Journal of the American Chemical Society. 122 (42). doi:10.1021/ja000921+.
  2. ^ Williams, Jonathan W.; Krynitsky, John A. (1941). "Acetoacetanilide". Organic Syntheses. 21: 4. doi:10.15227/orgsyn.021.0004.
  3. ^ Jaffe, Edward E. (2004). "Pigments, Organic". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.151807011001060605.a01.pub2. ISBN 978-0-471-48494-3.
  4. ^ K. Hunger. W. Herbst "Pigments, Organic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2012. doi:10.1002/14356007.a20_371
  5. ^ Lauer, W. M.; Kaslow, C. E. (1944). "4-Methylcarbostyril". Organic Syntheses. 24: 68. doi:10.15227/orgsyn.024.0068.