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Sterically Congested Molecules, 16 A Convenient Synthesis of Di-tert-butyl Ketone via its Imine, 2,2,4,4-tetramethyl-3-pentanimine

✍ Scribed by Knorr, Rudolf ;Donhärl, Angelika ;Hennig, Karsten-Olaf


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
272 KB
Volume
1996
Category
Article
ISSN
0947-3440

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✦ Synopsis


Abstract

2,2,4,4‐Tetramethyl‐3‐pentanimine (3) is efficiently prepared by a Barbier‐type reaction of pivalonitrile (1) with an excess of tert‐butyl chloride (2) and metallic lithium in ether. Its purification by extraction into aqueous acid and slow hydrolysis permit an inexpensive and very simple production of di‐tert‐butyl ketone (4).