期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 20, 期 8, 页码 1680-1689出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ob02168k
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资金
- National Natural Science Foundation of China [21972079]
- Natural Science Foundation of Shandong Province [ZR2019MB002]
- Shandong Provincial Natural Science Foundation [ZR2019LFG009]
- Incubation Program of Youth Innovation in Shandong Province
Direct metal-free deoxygenation of highly active allylic alcohols was achieved through catalysis by a Bronsted acid, avoiding tedious reaction steps and metal contamination. The system was found to be mainly suitable for aromatic allylic alcohols, with excellent yields obtained via gram-scale synthesis.
Direct metal-free deoxygenation of highly active allylic alcohols catalyzed by a Bronsted acid was achieved, which avoids tedious reaction steps and eliminates metal contamination. By examining a series of Bronsted acids, alcohols, reaction temperatures and so on, up to 94% yield was obtained with 10 mol% TsOH center dot H2O as the catalyst and 2 equiv. of p-methylbenzyl alcohol as the reductant at 80 degrees C for 2 h. The system was mainly suitable for aromatic allylic alcohols, and the yield was excellent as determined via gram-scale synthesis. The main product was double bond near the side of a more electron-rich aryl group when allylic alcohols featuring different substituents at the 1 and 3 positions were used as the substrates. Deuterium-labelled experiments clearly demonstrated that the hydrogen source was the methylene of p-methylbenzyl alcohol and other control experiments indicated the existence of two ether intermediates. Interestingly, in situ hydrogen transfer of allylic benzyl ether is a key process, but kinetic isotopic effect studies (k(H)/k(D) = 1.28) showed that the C-H bond cleavage was not the rate-determining step. A possible mechanism involving carbocations, ether intermediates and hydrogen transfer is proposed.
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