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. 2020 Jun 23;5(26):16010–16020. doi: 10.1021/acsomega.0c01413

Table 1. Alkaline Hydrolysis of Aryltriphenylphosphonium Bromides.

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a

Reaction conditions:18 reflux, 20% NaOH. The yields of Ph3PO are in the parentheses.

b

Reaction conditions:25 reflux, 1 M NaOH. nd = not detected.

c

Reaction conditions: phosphonium bromide 1 (0.5 mmol), 3 M NaOH (2 mL), rt, overnight or refluxed for 3 h.

d

PhCOOH was also isolated in 97% yield.

e

Phenanthracene was also isolated in 93%.