تفاعل #344843

ord-00e4528b56ff47a3a0972727d914fdb8

معادلة التفاعل

C1CCC2OC2C1
cyclohexene oxide
C[C](C)([K])c1ccccc1
α-cumylpotassium
CC(C)(c1ccccc1)[C@@H]1CCCC[C@H]1O
trans-2-cumylcyclohexanol
CC(C)(c1ccccc1)[C@@H]1CCCC[C@H]1O
racemic trans-2-(1-methyl-1-phenylethyl)cyclohexanol

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

الإجراء التجريبي

The next step in the synthesis was the addition of cyclohexene oxide to α-cumylpotassium to produce trans-2-cumylcyclohexanol. Dropwise addition of 105 mL (1.0 mol) of cyclohexene oxide (available from Lancaster Synthesis, Ltd., Windham, N.H., U.S.A.) followed; as before, the cyclohexene oxide addition was controlled so that the bath temperature did not rise above 30° C. As cyclohexene oxide was added, the reaction mixture thinned and became black. After this addition, the mixture was stirred for 3 hours. The reaction flask was cooled in an ice bath and 750 mL of saturated aqueous ammonium chloride was added slowly to the reaction mixture, which changed in color from light brown to bright orange to light brown again; concurrently, a white precipitate that had formed during the initial stages of the addition dissolved.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05262571uspto-grants-1993_11