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Di-/-butyl ketone

Di-w-butylcarbinol has been prepared by the action of M-butylmagnesium bromide upon m-valeraldehyde1 and upon ethyl formate.1,2 It has also been obtained by the catalytic hydrogenation of di- -butyl ketone in the presence of platinum.3... [Pg.62]

Di-/-butyl ketone reacts to yield pivalaldehyde, isobutylene, and 2-methylpropane. [Pg.168]

CAS 108-83-8 EINECS/ELINCS 203-620-1 UN 1157 (DOT) FEMA 3537 Synonyms DIBK Di butyl ketone s-Diisopropylacetone 2,6-Dimethyl-4-heptanone 2,6-Dimethylheptan-4-one Isobutyl ketone Isovalerone Valerone Classification Ketone Empirical CgHisO... [Pg.1354]

Many organic reagents have been used successfully in Pu separation processes. The reagents include tri- -butyl phosphate (TBP) methyl isobutyl ketone thenoyl ttifluoroacetone (TTA) ethers, eg, diethyl ether, di- -butyl ether, tetraethylene glycol dibutyl ether trdaurylamine (TT,A) trioctylamine (TOA) di- -butyl phosphate (DBP) hexyl-di(2-ethylhexyl) phosphate (HDEHP) and many others. Of these, TBP is by far the most widely used (30,95). [Pg.201]

In radical reactions not involving bromine or chlorine on the substrate, rearrangements are much rarer One example is the fluorination of di-tert butyl ketone which produces perfluormated / rt-buty isobutyl ketone [J5] Although isolated yields are poor only the rearranged ketone could be isolated This is perhaps only the second example of a 1,2-acyl shift Low fluorine substrate ratios show that this rearrangement occurs after monofluorination... [Pg.108]

The yields ranged from 55% for the mixture of enamines formed from morpholine and methylisopropyl ketone to 94% for the enamine formed from dimethylamine and methyl t-butyl ketone. The hindered ketone 2,5-dimethylcyclopentanone could be converted to an enamine, but the more hindered ketone, 2,6-di-t-butylcyclohexanone, was inert. White and Weingarten 43) attribute the effectiveness of titanium tetrachloride in this reaction to its ability to scavenge water and to polarize the carbonyl bond. [Pg.88]

X0 to hydroxy compounds. Lower temperatures favor ketone formation and sterically hindered carbonyls, such as 2-thienyl t-butyl ketone, are not reduced. The sensitivity of desulfurization to steric factors is evident by the failure to desulfurize 2,5-di-i-butyl-3-acetylthiophene. The carbonyl groups of both aldehydes and ketones can be protected by acetal formation, as particularly cyclic acetals are stable during desulfurization in methanol at room temperature. " The free aldehydes give primary alcohols on desulfurization. Another method to obtain only keto compounds is to oxidize the mixtures of ketone and secondary alcohol with CrOs after the desulfurization. - Through the desulfurization of 5,5 -diacetyl-2,2, 5, 2"-terthienyl (228), 2,15-hexadecandione (229) has been obtained, which... [Pg.112]

Methyl n-amyl carbinol from methyl n-amyl ketone) Methyl n-butyl carbinol from methyl n-butyl ketone) Methyl t o-propyl carbinol Di-n-butyl carbinol from n-butyl bromide)... [Pg.1203]

Di-f-butyl ketone reacts in pentane solution to yield the following products<14) ... [Pg.78]

Methyl ethyl ketone Diethyl ketone Diisopropyl ketone Di-f-butyl ketone Benzophenone... [Pg.130]

Lomas and Dubois (113a) treated di-rerf-butyl ketone with o-tolyllithium and obtained a mixture of rotamers of o-tolyl-di-terf-butylcarbinol (74), which were... [Pg.45]

I) Acetaldehyde, Acetone, Di-tert-butyl ketone. Methyl tert-butyl ketone (reactivity towards HCN)... [Pg.109]

Di-n-butyl ketone n-Butyl bromide Tri-n-butyl carbinol 91... [Pg.12]

Values of 1554 cm for the carbonyl stretching frequency in tlie radical-anion of benzophenone [16] and of 1558 cm for the radical-anion of di-ter/.-butyl ketone [17] suggest that in general Vco will be found at lower frequencies for the radical-anion than for the parent carbonyl compound. [Pg.332]

Surprisingly, under these conditions di-ferf-butyl ketone hydrazone afforded 1,1-di-ferf-butyltetrathiolane in very low yield (2%) (see similar reaction in Scheme 91). [Pg.220]

Jones and Knochel found that the adduct of allylzinc bromide and di-i-butyl ketone, upon conversion to the bromozinc alkoxide, serves as a source of allylzinc bromide,... [Pg.423]


See other pages where Di-/-butyl ketone is mentioned: [Pg.283]    [Pg.30]    [Pg.182]    [Pg.553]    [Pg.297]    [Pg.165]    [Pg.1785]    [Pg.283]    [Pg.30]    [Pg.182]    [Pg.553]    [Pg.297]    [Pg.165]    [Pg.1785]    [Pg.346]    [Pg.346]    [Pg.184]    [Pg.436]    [Pg.111]    [Pg.111]    [Pg.113]    [Pg.113]    [Pg.106]    [Pg.107]    [Pg.346]    [Pg.346]    [Pg.78]    [Pg.499]    [Pg.239]    [Pg.1729]    [Pg.84]    [Pg.181]    [Pg.851]    [Pg.50]    [Pg.50]   
See also in sourсe #XX -- [ Pg.31 , Pg.35 ]




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Butyl Ketone

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