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Isolating Methods
Soxhletting the root bark of cinnamomum camphora (camphor laurel), or probably parts of other plants (see below) with distilled ethanol, or hexane and chloroform, yields most of the available safrole, and is cheap and effective. The solvents can be evaporated off or reclaimed by distillation.
Dealing with the impurities in the soxhlet extract is another matter. Steam distillation from bulk plant material is also reported to work.
Refinement methods from oil
Cool the oil or the safrole-containing fraction of the oil, to at least -12°C. Safrole will crystallise.
Use fractional distillation, followed by cooling and crystallisation. Regarding the distillation of safrole in mixtures consult Brauer, Ber Schimmel & Co, Jubil?ms-Ausgabe (1929), 153.
Where safrole may be contaminated by oily constituents in an essential oil as in red camphor oil, the method of Ikeda and Takeda (a) may be employed advantageously to determine the safrole by reparation of the addition product with mercuric acetate and sodium chloride in dilute acetone. The precipitate so formed should be filtered in a Gooch funnel and weighed, and used with a correction factor to define the percentage of safrole in the sample. This complex hydroxychloride of safrole [C10H10O2(OH)HgCl] according to Tsukamoto (b) is readily decomposed to regenerate safrole either by sodium sulfide and zinc in potassium hydroxide; or hydrochloric acid. The oxychloride melts at 141-142°C according to Fujita (c).
Safrole will convert to allylpyrocatechol when heated with phosphoric acid. Safrole is oxidised to piperonylic acid (mp 238°C) by the action of potassium permanganate in aqueous acetone. Some piperonylacetic acid (mp 87-88°C) is also produced. Safrole is oxidised to piperonal (heliotropin, mp 38°C) by the action of potassium dichromate and dilute sulfuric acid. Safrole isomerises to isosafrole when heated with alkalis. See also step (3) in isolation, above.
Isosafrole (120-58-1)
Isosafrole is technically a member of the styrenes and polymerises under the influence of acids. It is soluble in ethanol, ether, benzene and is steam-volatile. It shares safrole's empirical formula and molecular weight. Isosafrole exists in two isomeric forms, the cis- isomer and the more energetically favourable trans-isomer. Warming converts the cis-form to the trans-configuration. Isosafrole is not as widely distributed in nature as safrole. It is best purified via a picrate derivative, the trans- isomer of which has mp 74.75°C. The picrate cis- isomer melts at 68.5°C.
Cis-isosafrole boils at 253°C at 760mmHg; 179.5°C at 100mmHg.
Trans-isosafrole melts at 6.7-6.8°C and boils at 247-247°C.
Trans-isosafrole has a density of 1.122g/cc.