Adding a certain compound to certain chemical reactions, such as: 4415-82-1, Cyclobutylmethanol, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound, 4415-82-1, blongs to alcohols-buliding-blocks compound. name: Cyclobutylmethanol
Example 37: (E)-3-(cyclobutylmethylene)octan-2-one (Compound ID 19) Prepared as described in Example 35 in 50% yield from cyclobutanecarbaldehyde (obtained by PCC-oxidation of cyclobutanemethanol) and diethyl 2-oxooctan-3- ylphosphonate (obtained from hexyl iodide and triethyl phosphite via diethyl hexylphosphonate). Boiling point: 105C (0.07 mbar).13C-NMR (100MHz, CDCI3): £199.75 (s, C(2)), 147.99 (d, CH=C(3)), 140.66 (s, C(3)), 34.82 (Cf), 31.92 (Q, 29.33 (Q, 29.20 (t, 2 C), 25.66 (Q, 25.61 (q, C(I)), 22.50 (Q, 19.05 (Q, 13.97 t°, C(S)).MS (El): 194 (2), 179 (7), 166 (16), 151 (11), 137 (29), 123 (44), 109 (39), 95 (27), 81 (27), 79 (13), 77 (8), 67 (30), 55 (13), 43 (100).
These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,4415-82-1, its application will become more common.
Reference:
Patent; GIVAUDAN SA; WO2008/116338; (2008); A2;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts