2-重氮基环戊酮 以 氯仿 用作溶剂,化学反应 0.17H,反应生成环丁烷甲酸乙酯
参考文献:Direct Observation Of .Alpha.-Oxo Ketenes From The Photolysis Of .Alpha.-Diazo .Beta.-Diketones
标题:Direct Observation Of .Alpha.-Oxo Ketenes From The Photolysis Of .Alpha.-Diazo .Beta.-Diketones
摘要:Monitoring By Ir Spectroscopy Of The Broad-Band Irradiation Of The Symmetrically Substituted 2-Diazo-Cyclohexane-1,3-Dione (I 1),3-Diazopentane-2,4-Dione (19),And 4-Diazo-2,2,6,6-Tetramethylheptane-3,5-Dione (24) In Ar Matrices At 12 K Showed The Formation Of 2-Carbonylcyclopentanone (S-Z-12),Acetyl(Methyl)Ketene (S-E-20),And Tert-Butyl(Pivaloyl)Ketene (S-E-25),Respectively,In Less Than 10 Min. On Increasing The Photolysis Time To >3 H,The Alpha-Oxo Ketenes 12,20,And 25 Decarbonylated To The Corresponding Oxocarbenes Which Underwent Wolff Rearrangement To Carbonylcyclobutane (15),Dimethylketene (23),And Di-Tert-Butylketene (28),Respectively. The Reaction Of 2-Carbonylcyclopentanone (12) With Ch3Oh Was Monitored By Ir Spectroscopy. Thus,It Was Found That The Reaction Started At Ca. 100 K And Was Essentially Complete At 140 K,Involving The Initial Formation Of The Enol Form (9) Of Methyl 2-Oxocyclopentanecarboxylate.
Doi:10.1021/jo00044A019