作者:Yasuo Kikugawa、Liang Hua Fu、Takeshi Sakamoto
DOI:10.1080/00397919308018582
日期:1993.4
Abstract N-Methoxy imidoyl bromides are synthesized in one-pot from the carboxylic acids with methoxyamine and triphenylphosphine-tetrabromomethane. Photolysis of them leads to formation of the corresponding nitriles in high yield without affecting functional groups sensitive to ordinary dehydrating and halogenating reagents.
摘要 以羧酸为原料,以甲氧基胺和三苯基膦-四溴甲烷为原料,一锅法合成了N-甲氧基亚氨基溴化物。它们的光解导致以高产率形成相应的腈,而不会影响对普通脱水和卤化试剂敏感的官能团。