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. 2016 Aug 16;4:35. doi: 10.3389/fchem.2016.00035

Table 2.

Synthesis of substituted benzyl phosphonates in PEG-400a.

Entry Benzyl halide Product Yieldb (%)
1 graphic file with name fchem-04-00035-i0001.jpg 9842
2 graphic file with name fchem-04-00035-i0002.jpg 9243
3 graphic file with name fchem-04-00035-i0003.jpg 8942
4 graphic file with name fchem-04-00035-i0004.jpg 9142
5 graphic file with name fchem-04-00035-i0005.jpg 8844
6 graphic file with name fchem-04-00035-i0006.jpg 9345
7 graphic file with name fchem-04-00035-i0007.jpg 9846
8 graphic file with name fchem-04-00035-i0008.jpg 9147
9 graphic file with name fchem-04-00035-i0009.jpg 9047
10 graphic file with name fchem-04-00035-i0010.jpg 9347
11 graphic file with name fchem-04-00035-i0011.jpg 9048
12 graphic file with name fchem-04-00035-i0012.jpg 9448
13 graphic file with name fchem-04-00035-i0013.jpg 8249
a

Reaction Conditions: benzyl halide (1 mmol) and dialkyl phosphite (1 mmol), K2CO3 (2 mmol), KI (0.3 mmol), PEG (0.5 g), RT (28°C), 6 h.

b

Isolated Yield.