(2R)-2-[(2-methylpropan-2-yl)oxymethyl]oxirane

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

Procedure: Using N,N-dimethylformamide solution of isobutyl-2-(2-methoxyphenoxy)ethylcarbamate 53.46 g (0.2 mol), lithium-t-butoxide 3.2 g (0.04 mol) and (R)-2-t-butoxymethyl-oxiran 28.6 g (0.22 mol), the procedures as described in Example 1 were carried out to obtain the targeted product. to obtain the targeted product

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

Procedure: Using N,N-dimethylformamide solution of isobutyl-2-(2-methoxyphenoxy)ethylcarbamate 53.46 g (0.2 mol), lithium-t-butoxide 3.2 g (0.04 mol) and (R)-2-t-butoxymethyl-oxiran 28.6 g (0.22 mol), the procedures as described in Example 1 were carried out to obtain the targeted product. to obtain the targeted product

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

Procedure: Using N,N-dimethylformamide solution of isobutyl-2-(2-methoxyphenoxy)ethylcarbamate 53.46 g (0.2 mol), lithium-t-butoxide 3.2 g (0.04 mol) and (R)-2-t-butoxymethyl-oxiran 28.6 g (0.22 mol), the procedures as described in Example 1 were carried out to obtain the targeted product. to obtain the targeted product