反应详情
EQUATION
反应方程式
REACTANTS
反应物
Hydroxide
HO-
Methyl vinyl ketone
C4H6O
2,3,6-Trimethylphenol
C9H12O
N,N,N-Trimethyl-3-oxobutan-1-aminium iodide
C7H16INO
4-Chlorobutan-2-one
C4H7ClO
2-Butanone, 4-hydroxy-
C4H8O2
2-Butanone, 4-methoxy-
C5H10O2
2-Butanone, 4-(acetyloxy)-
C6H10O3
Hydride
H-
未命名化合物
2-Butanone, 4-(benzoyloxy)-
C11H12O3
2-Butanone, 4-phenoxy-
C10H12O2
未命名化合物
未命名化合物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A process for the production of 2,3,6-trimethylphenol which comprises reacting a carbonyl compound selected from the group consisting of methyl vinyl ketone, methyl β-hydroxyethyl ketone, methyl β-methoxyethyl ketone, methyl β-phenoxyethyl ketone, methyl β-acetyloxyethyl ketone, methyl β-benzoyloxyethyl ketone, methyl β-methyl-sulfonyloxyethyl ketone, methyl β-phenylsulfonyloxyethyl ketone, methyl β-dimethylaminoethyl ketone, methyl β-chloroethyl ketone, dimethyl-(β-acetylethyl)-sulfonium bromide or trimethyl-(β-acetylethyl)-ammonium iodide to a mixture of diethyl ketone and a basic reagent selected from the group consisting of an alkali metal, an alkaline earth metal, a hydroxide, oxide, alcoholate, amide, hydride or organo metallic compound of an alkali metal or alkaline earth metal, and a quaternary ammonium hydroxide, the amount of said diethyl ketone being in the molar ratio of 1:1 to 50:1 with respect to the total amount of carbonyl compound added, at a reaction temperature of 20° to 150° C. to produce 2,3,6-trimethyl-2-cyclohexen-1-one, and dehydrogenating the latter to produce 2,3,6-trimethylphenol.