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Alcohols from Grignard reactions

A great many alcohols can be obtained from Grignard reactions, depending on the reactants. For example, Grignard reagents react with formaldehyde,... [Pg.669]

This preparation is an example of the use of di-M-butyl ether as a solvent in the Grignard reaction. The advantages are it is comparatively inexpensive, it can be handled without excessive loss due to evaporation, simple distillation gives an ether free from moisture and alcohol, and the vapour does not form explosive mixtures with air. n-Butyl ether cannot, of course, be employed when the boiling point of the neutral reaction product is close to 140°. [Pg.254]

Alcohols from Reaction of Carbonyl Compounds with Grignard Reagents 613... [Pg.613]

The mechanism of this Grignard reaction is similar to that of L1AIH4 reduction. The first equivalent of Grignard reagent adds to the acid chloride, loss of (T from the tetrahedral intermediate yields a ketone, and a second equivalent of Grignard reagent immediately adds to the ketone to produce an alcohol. [Pg.805]

Halo-l-benzothiepins 4 can be synthesized by the treatment of 7a-halobenzo[fe]cyclopropa-[e]thiopyran-7-ols 2 with hydrogen bromide and subsequent hydrogen bromide elimination from the 2,4-dihalo-2,3-dihydro-l-benzothiepins 3 by l,5-diazabicyclo[4.3.0]non-5-ene (DBN).9 The alcohols 2 are prepared by Grignard reaction of the corresponding 7a-halobenzo[ft]cyclopropa[c]thiopyran-7-ones l18 and are used for the synthesis without purification. The intermediate dihalodihydro-l-benzothiepins 3 are not isolated due to their thermal lability related and more stable compounds are described in Section 2.1.2.1. [Pg.80]

Remember, however that CHAOS does not intend to be a database of "synthetic methods" presently available to organic chemists. CHAOS is aimed at finding the intermediate precursors of the "synthesis tree" by means of selected basic disconnections (either "consonant" or "dissonant"). In the author s view, it is of minor importance, for instance, how a "carbene" -resulting from a -(2 + 1) cycloelimination- is generated, or whether a double bond is the direct result of a Wittig reaction or the dehydration of an alcohol formed in a Grignard reaction. In... [Pg.427]


See other pages where Alcohols from Grignard reactions is mentioned: [Pg.637]    [Pg.580]    [Pg.637]    [Pg.47]    [Pg.557]    [Pg.637]    [Pg.314]    [Pg.659]    [Pg.951]    [Pg.416]    [Pg.46]    [Pg.394]    [Pg.244]    [Pg.34]    [Pg.387]    [Pg.156]    [Pg.394]    [Pg.143]    [Pg.615]    [Pg.1290]    [Pg.97]    [Pg.333]    [Pg.391]    [Pg.378]    [Pg.379]    [Pg.293]    [Pg.653]    [Pg.143]    [Pg.41]    [Pg.450]    [Pg.79]    [Pg.301]    [Pg.134]   
See also in sourсe #XX -- [ Pg.201 ]




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Acid chloride, alcohols from Grignard reaction

Acid chloride, alcohols from reaction with Grignard reagents

Alcohols Grignard

Alcohols from Carbonyl Compounds Grignard Reaction

Alcohols from Reaction of Carbonyl Compounds with Grignard Reagents

Grignard reaction alcohols

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