Isopropenyl acetate

Isopropenyl acetate
Names
	Other names 1-Methylvinyl acetate
Identifiers
CAS Number	108-22-5;
3D model (JSmol)	Interactive image;
ChemSpider	7628;
EC Number	203-562-7
PubChem CID	7916;
	InChI InChI=1S/C5H8O2/c1-4(2)7-5(3)6/h1H2,2-3H3 Key: HETCEOQFVDFGSY-UHFFFAOYSA-N;
	SMILES CC(=C)OC(=O)C;
Properties
Chemical formula	C5H8O2
Molar mass	100.12 g·mol−1
Appearance	Colorless liquid
Density	0.9090 g/cm3 (20 ºC)
Melting point	−92.9 °C (−135.2 °F; 180.2 K)
Boiling point	97 °C (207 °F; 370 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Isopropenyl acetate is an organic compound, which is the acetate ester of the enol tautomer of acetone. This colorless liquid is significant commercially as the principal precursor to acetylacetone. In organic synthesis, it is used to prepare enol acetates of ketones and acetonides from diols.^[1]

Preparation and reactions

Isopropenyl acetate is prepared by treating acetone with ketene.^[2] Upon heating over a metal surface, isopropenyl acetate rearranges to acetylacetone.^[3]

CH₂(CH₃)COC(O)Me → MeC(O)CH₂C(O)Me

References

↑ Michael A. Walters, Melissa D. Lee (2001). "Isopropenyl Acetate". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.ri077.
↑ Raimund Miller, Claudio Abaecherli, Adel Said, Barry Jackson "Ketenes" in Ullmann's Encyclopedia of Industrial Chemistry, 2001, Wiley-VCH, Weinheim. doi:10.1002/14356007.a15_063
↑ Siegel, Hardo; Eggersdorfer, Manfred (2002). "Ketones". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a15_077.

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[1] Michael A. Walters, Melissa D. Lee (2001). "Isopropenyl Acetate". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.ri077.

[2] Raimund Miller, Claudio Abaecherli, Adel Said, Barry Jackson "Ketenes" in Ullmann's Encyclopedia of Industrial Chemistry, 2001, Wiley-VCH, Weinheim. doi:10.1002/14356007.a15_063

[3] Siegel, Hardo; Eggersdorfer, Manfred (2002). "Ketones". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a15_077.