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2-(2-BroMocyclohex-1-en-1-yl)ethan-1-ol synthesis

3synthesis methods
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Yield:85236-15-3 82%

Reaction Conditions:

Stage #1: 1-Bromo-2-ethenylcyclohex-1-enewith 9-bora-bicyclo[3.3.1]nonane in tetrahydrofuran at 20; for 26 h;Inert atmosphere;
Stage #2: with dihydrogen peroxide;sodium hydroxide in tetrahydrofuran;methanol; for 3 h;Reflux;

References:

Zhan, Fuxu;Liang, Guangxin [Angewandte Chemie - International Edition,2013,vol. 52,# 4,p. 1266 - 1269][Angew. Chem.,2012,vol. 125,# 4,p. 1304 - 1307,4] Location in patent:supporting information