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0342745088
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note
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Preparation of 2-methyl-1,8-octanediol (8): The DIBAL-H reduction of ε-caprolactone followed by Wittig reaction with triethyl 2-phosphono propionate afforded ethyl 8-hydroxy-2-methyl-2-octenoate in 90% yield (two steps). The ester was hydrogenated (Pd/C) and reduced by DIBAL-H to give 8 in 78% yield (two steps).
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