Benazaldehyde to $\alpha$-Hydroxyphenylacetic acid.
Benazaldehyde to $\alpha$-Hydroxyphenylacetic acid.
$\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{OH}\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{OH}\\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ |\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ |\\ \text{C}_6\text{H}_5\text{CHO}\xrightarrow[\text{pH. 9-10}]{\text{HCN}}\text{C}_6\text{H}_5\text{CH}-\text{CN}\xrightarrow{\text{H}^+/\text{H}_2\text{O}}\text{C}_6\text{H}_5-\text{CH}-\text{COOH}$
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Reimer-Tiemann reaction.
$\text{C}_6\text{H}_5\text{N}_2\text{Cl}+\text{H}_3\text{PO}_2+\text{H}_2\text{O}\rightarrow$