2-cyclohexylpropan-2-ol

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The following compounds were prepared analogously to the method described in Example 16, except that the alcohol component used was 2-(3,3-dimethylcyclohexyl)-2-propanol, [which can be prepared from methylmagnesium chloride and 1-(3,3-dimethylcyclohexyl)-ethanone by a Grignard reaction] instead of 2-cyclohexyl-2-propanol. The esterification was carried out with acetic anhydride (Example 18) or propionic anhydride (Example 19). Thus, only the spectroscopic data are indicated at this point: The following compounds were prepared analogously to the method

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The following compounds of Examples 6 and 7 were prepared analogously to the methods described under Example 1, except that the alcohol component used was 2-cyclohexyl-2-propanol, which can be prepared from cyclohexylmagnesium chloride and acetone by a Grignard reaction, instead of 1-cyclohexyl-1-ethanol. Furthermore, propylene oxide was used instead of isobutylene oxide. The esterification was carried out with acetic anhydride (Example 6) or propionic anhydride (Example 7). Thus, only the spectroscopic data are given at this point: