Preparation and Some Reactions of Dimethyl(trimethylsilylimino)silane, Me2SiNSiMe3
โ Scribed by Prof. Dr. Nils Wiberg; Dipl.-Chem. Gerhard Preiner
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 236 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
โฆ Synopsis
H20 7 H3 (4) + 2 [CO'Pcj--2 COI'PC + c1-+ c12c=c I + HC03-+ ( 3 ) c H3 C o P c = Cobalt phthalocyanine
Removal of the TCBOC group can be accomplished with the supernucleophilic cobalt(1)-phthalocyanine anion in methanol or a~etonitrile[~, '3 and with zinc in glacial acetic acid (see Table ); the yields of amine component are 66-94 %.
N-Terminal deprotection by lithium cobalt(1)-phthalocyanine also proceeds smoothly in the case of benzyl esters.
๐ SIMILAR VOLUMES
1-Trimethylsiloxyalkyl-bis(trimethylsilyl)silanes ( 5), obtained by a base induced isomerization of easily accessable 1-hydroxyalkyl-tris(trimethylsilyl)silanes (1) were hydrolized to give 1-hydroxyalkyl-bis(trimethylsilyl)silanes ( 6), which in presence of sodium hydride underwent a further 1,3-Si,
Reactions of morpholine in dimethyl sulphoxide at unsubstituted ring positions of 1,3,5-trinitrobenzene, and phenyl 2,4,64rinitrophenyl ether, yield anionic a-adducts via zwitterionic intermediates. Reactions at the 1- position of phenyl 2,4,64rinitrophenyl ether, phenyl 2,4-dinitronaphthyl ether, a