Functionalized ketones by iron mediated reaction of grignard reagents with acyl chlorides
β Scribed by C. Cardellicchio; V. Fiandanese; G. Marchese; L. Ronzini
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 219 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The iron(:II)-catalyzed cross-coupling reaction between Grignard reagents and acyl ___chlorides was found to be widely applicable to the synthesis of various functionalized ketones in good yields under mild conditions; the series of examples includes the synthesis of chiral methyl ketones and symmetric diketones.
In a previous work', we have reported a simple and versatile synthesis leading to ketones in high yields and without concomitant formation of alcohols.
The procedure involves a
π SIMILAR VOLUMES
TABLE Cross-Coupling Reactions of Acyl Chlorides with Grignard Reagents in the Presence of Fe(acac)3 as a Catalysta. R-C+ 0 3% Fe(acac)3 0 + 'Cl R'MgXb THF R-C< R' Entry R R' Temp Yield in KetoneC % 1 CH3(Ct& CH3 r.t. 84 2 CH3(CH2)4 CH3(C"2)4 r.t. 82 3 CH3 CH3(CH2)8 r.t. 82 4 CH3 CH3(CH2)9 r.t. 80 5
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