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・ 3-Methoxy-4-hydroxyphenylglycol
・ 3-Methoxy-4-methylamphetamine
・ 3-Methoxyamphetamine
・ 3-Methoxymethamphetamine
・ 3-Methoxymorphinan
・ 3-Methoxytyramine
・ 3-Methyl-1-pentanol
・ 3-Methyl-2-butanol
・ 3-methyl-2-oxobutanoate dehydrogenase
・ 3-Methyl-2-oxobutanoate dehydrogenase (acetyl-transferring) kinase
・ 3-methyl-2-oxobutanoate dehydrogenase (ferredoxin)
・ 3-methyl-2-oxobutanoate hydroxymethyltransferase
・ 3-Methyl-2-pentanol
・ 3-Methyl-2-pentanone
・ 3-Methyl-3-octanol
3-Methyl-3-pentanol
・ 3-Methyl-3-penten-2-one
・ 3-Methyl-4-octanolide
・ 3-Methylamphetamine
・ 3-methylbutanal reductase
・ 3-Methylbutanoic acid
・ 3-Methylbutyrfentanyl
・ 3-Methylcatechol
・ 3-Methylcrotonyl-CoA carboxylase deficiency
・ 3-Methylcyclopropene
・ 3-methyleneoxindole reductase
・ 3-Methylfentanyl
・ 3-Methylfuran
・ 3-Methylglutaconic acid
・ 3-Methylglutaconic aciduria


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3-Methyl-3-pentanol : ウィキペディア英語版
3-Methyl-3-pentanol

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3-Methyl-3-pentanol (IUPAC name) is an organic chemical compound and a tertiary hexanol. It is used in the synthesis of the tranquilizer emylcamate.〔

== Synthesis ==
It can be prepared by reacting ethylmagnesium bromide with ethyl acetate in the so called Grignard reaction using dried diethyl ether or tetrahydrofuran as solvent. It can be prepared also by reacting ethylmagnesium bromide with butanone in the same conditions already mentioned.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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