Oxirane, (phenoxymethyl)-

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Reaction thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

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Individual Reactions

2-Propanol, 1-phenoxy-3-(phenylamino)- = Oxirane, (phenoxymethyl)- + Aniline

By formula: C15H17NO2 = C9H10O2 + C6H7N

Quantity Value Units Method Reference Comment
Δr113. ± 2.kJ/molCmKuznetsova, Rakova, et al., 1975solid phase; solvent: DMF

Benzene, isocyanato- + Oxirane, (phenoxymethyl)- = 5-Phenoxymethyl-3-phenyl-2-oxazolidone

By formula: C7H5NO + C9H10O2 = C16H15NO3

Quantity Value Units Method Reference Comment
Δr-196.7kJ/molCmLebedev, Bykova, et al., 1988liquid phase

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Kuznetsova, Rakova, et al., 1975
Kuznetsova, V.P.; Rakova, G.V.; Miroshnichenko, E.A.; Lebedev, Yu.A.; Enikolopyan, N.S., Thermochemical study of the interaction of epoxy compounds with primary amines, Dokl. Phys. Chem. (Engl. Transl.), 1975, 225, 1231-1234. [all data]

Lebedev, Bykova, et al., 1988
Lebedev, B.V.; Bykova, T.A.; Kiparisova, E.G.; Frenkel, Ts.M.; Fainleib, A.M.; Pankratov, V.A., Thermodynamics of phenyl glycidyl ether and its reactions with diphenylcarbodiimide and phenyl isocyanate with the formation of iminooxazolidine and oxazolidinone in the 0-330 K range, Bull. Acad. Sci. USSR, Div. Chem. Sci., 1988, 1082-10. [all data]


Notes

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