Abstract
Synthesis of two solid derivatives of vitamin K3 (2-methylnaphthalene-1,4-dione or menadione), 2-(benzylamino)-3-methylnaphthalene-1,4-dione and 3-(phenethylamino)-2-methylnaphthalene-1,4-dione was completed using a 1,4 Michael addition reaction at 323K in an inert atmosphere, with reaction yields of 62% mol·mol−1 and 71% mol·mol−1, respectively, and a purity grade of 98% mol·mol−1 for each component. Isothermal solubility (mole fraction) of each solid derivative in supercritical carbon dioxide was performed using an analytic-recirculation methodology, with direct determination of the molar composition of the carbon dioxide-rich phase by using high performance liquid chromatography, at temperatures of (313, 323 and 333)K and pressures from (8–28)MPa. Results indicated that the range of measured solubilities were from (59×10−6 to 368×10−6)mol·mol−1 for solid 2-(benzylamino)-3-methylnaphthalene-1,4-dione and from (40×10−6 to 205×10−6)mol·mol−1 for solid 3-(phenethylamino)-2-methylnaphthalene-1,4-dione. The experimental solubility was validated using three approaches, estimating the combined expanded uncertainty of measurement for each solubility data point, evaluating the thermodynamic consistency of the data utilizing a test based on the Gibbs–Duhem equation, and verifying the self-consistency by correlating the experimental solubility values with a semi-empirical model as a function of temperature, pressure and pure carbon dioxide density.
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