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. 2023 Sep 4;28(17):6434. doi: 10.3390/molecules28176434

Table 1.

Results of the reactions of resorcinols and naphthols with citronellal a.

graphic file with name molecules-28-06434-i001.jpg
Entry Starting Material Citronellal Product Yield (%)
1 graphic file with name molecules-28-06434-i002.jpg 9a graphic file with name molecules-28-06434-i003.jpg 68
2 graphic file with name molecules-28-06434-i004.jpg 9a graphic file with name molecules-28-06434-i005.jpg 87
3 graphic file with name molecules-28-06434-i006.jpg 9a graphic file with name molecules-28-06434-i007.jpg 75
3 graphic file with name molecules-28-06434-i008.jpg 9a graphic file with name molecules-28-06434-i009.jpg 92
4 graphic file with name molecules-28-06434-i010.jpg 9a graphic file with name molecules-28-06434-i011.jpg 72
5 graphic file with name molecules-28-06434-i012.jpg 9b graphic file with name molecules-28-06434-i013.jpg 70
6 graphic file with name molecules-28-06434-i014.jpg 9b graphic file with name molecules-28-06434-i015.jpg 87
7 graphic file with name molecules-28-06434-i016.jpg 9b graphic file with name molecules-28-06434-i017.jpg 90
8 graphic file with name molecules-28-06434-i018.jpg 9b graphic file with name molecules-28-06434-i019.jpg 75

a Reaction conditions: starting material (1.0 mmol), citronellal (1.5 mmol), EDDA (20% mol), TEA (0.2% mol) in xylene [21].