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(5R)-2-Methylene-5-(1-methylethenyl)cyclohexanol (Mixture of Diastereomers) synthesis

4synthesis methods
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Yield:216655-61-7 96%

Reaction Conditions:

Stage #1: (4R)-limonene 1,2-epoxidewith diethyl(2,2,6,6-tetramethylpiperidino)aluminium in hexane;benzene at 0 - 20; for 2.75 h;Yamamoto rearrangement;
Stage #2: with sodium hydrogencarbonate in hexane;benzene at 0;Saturated solution;

References:

Uroos, Maliha;Lewis, William;Blake, Alexander J.;Hayes, Christopher J. [Journal of Organic Chemistry,2010,vol. 75,# 24,p. 8465 - 8470] Location in patent:experimental part