化学
甲酸钠
一氧化碳
芳基
催化作用
钯
卤化物
甲酰化
格式化
有机化学
无机化学
烷基
作者
Tamon Okano,Nobuyuki Harada,Jitsuo Kiji
摘要
Abstract The formylation of aryl bromides or iodides with HCOONa at atmospheric pressure of CO readily proceeded in the presence of PdCl2(PPh3)2 in DMF to afford the corresponding aldehydes in good yields. The contamination with water promoted a side reaction to form carboxylic acids. The formylation using HCOOK or HCOONH4 as a hydride source was fast but gave a considerable amount of the reduction product.
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