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Grignard reagents from alkyl halide reduction

Alkanes can also be prepared from alkyl halides by reduction, directly with Zn and acetic acid (AcOH) (see Section 5.7.14) or via the Grignard reagent formation followed by hydrolytic work-up (see Section 5.7.15). The coupling reaction of alkyl halides with Gilman reagent (R 2CuLi, lithium organocuprates) also produces alkanes (see Section 5.5.2). [Pg.68]

Reduction of carbon-halogen bond by metal yields carbanion. Reaction of alkyl halide with Mg in the presence of anhydrous ether as solvent generates Grignard reagent. The Grignard reagent behaves like a carbanion. Alkyllithiums are also obtained from alkyl halides and behave as carbanions. [Pg.65]

Several thiols occur naturally for example, skunk secretion contains 3-methyll-butanethiol and cut onions evolve 1-propanethiol, and the thiol group of the natural amino acid cysteine plays a vital role in the biochemistry of proteins and enzymes (see Introduction, p. 2). Primary and secondary thiols may be prepared from alkyl halides (RX) by reaction with excess sodium thiolate (SN2 nucleophilic substitution by HST) or via the Grignard reagent and reaction with sulfur. Tertiary thiols can be obtained in good yields by addition of hydrogen sulfide to a suitable alkene. Thiols can also be prepared by reduction of sulfonyl chlorides (Scheme l).la,2a... [Pg.47]

Sulfides, or thioethers, are sulfur analogues of ethers, and like ethers they can be either symmetrical (R2S) or unsymmetrical (RSR1, where R and R are different). Sulfides can be prepared from alkyl halides by a Williamson-type synthesis with sodium hydrogen sulfide, sodium thiolate or sodium sulfide from alkyl or aryl halides via the Grignard reagent (11) from alkenes by radical-catalysed addition of thiols or by reduction of sulfoxides (Scheme 9).2b... [Pg.50]

Organocadmium compounds can be prepared from Grignard reagents or organo-lithium compounds by reaction with Cd(II) salts.180 They can also be prepared directly from alkyl, benzyl, and aryl halides by reaction with highly reactive cadmium metal generated by reduction of Cd(II) salts.181... [Pg.661]


See other pages where Grignard reagents from alkyl halide reduction is mentioned: [Pg.188]    [Pg.35]    [Pg.237]    [Pg.259]    [Pg.167]    [Pg.23]    [Pg.80]    [Pg.76]    [Pg.73]    [Pg.861]    [Pg.380]    [Pg.315]    [Pg.495]    [Pg.1233]    [Pg.255]    [Pg.257]    [Pg.168]    [Pg.733]    [Pg.145]    [Pg.201]    [Pg.73]    [Pg.132]    [Pg.209]    [Pg.528]    [Pg.109]    [Pg.109]    [Pg.87]    [Pg.238]    [Pg.297]    [Pg.733]    [Pg.651]   
See also in sourсe #XX -- [ Pg.579 ]




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Alkyl Grignard reagents

Alkyl Grignards

Alkyl reagents

Alkyl reduction

Alkylating reagents

From Grignard reagents

From alkyl halides

Grignard reagents from alkyl halides

Grignard reduction

Halides reagents

Halides reduction

Halides, alkyl reduction

Reagent alkyl halides

Reagents alkylation

Reduction alkylation

Reduction reagents

Reduction reductive alkylation

Reductive alkylation

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