Technology Process of C54H65N5O9Si2
There total 3 articles about C54H65N5O9Si2 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 60 percent / pyridinium dichromate / dimethylformamide
2: NaOH
3: 1.) N-methylmorpholine, O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate, N-hydroxybenzotriazole, 2.) N-methylmorpholine / 1.) acetonitrile, r.t., 0.5 h, 2.) acetonitrile, r.t., 20 h
With
4-methyl-morpholine; sodium hydroxide; dipyridinium dichromate; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate;
In
N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 2 steps
1: NaOH
2: 1.) N-methylmorpholine, O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate, N-hydroxybenzotriazole, 2.) N-methylmorpholine / 1.) acetonitrile, r.t., 0.5 h, 2.) acetonitrile, r.t., 20 h
With
4-methyl-morpholine; sodium hydroxide; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate;
- Guidance literature:
-
With
4-methyl-morpholine; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate;
Yield given. Multistep reaction;
1.) acetonitrile, r.t., 0.5 h, 2.) acetonitrile, r.t., 20 h;