Technology Process of C23H28FN5O5Si
There total 6 articles about C23H28FN5O5Si which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
C23H30FN5O4Si;
With
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium hydrogencarbonate; acetic acid;
In
water; acetonitrile;
at 22 - 40 ℃;
for 0.25h;
With
[bis(acetoxy)iodo]benzene; acetic acid;
In
water; acetonitrile;
at 22 ℃;
for 0.25h;
pH=6.5 - 7;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: N-ethyl-N,N-diisopropylamine / toluene / 50 °C
2.1: toluene-4-sulfonic acid / toluene; methanol / 0 °C
3.1: sodium hydrogencarbonate; acetic acid; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / acetonitrile; water / 0.25 h / 22 - 40 °C
3.2: 0.25 h / 22 °C / pH 6.5 - 7
With
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium hydrogencarbonate; toluene-4-sulfonic acid; acetic acid; N-ethyl-N,N-diisopropylamine;
In
methanol; water; toluene; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: hydrogen bromide; acetic acid / dichloromethane / 0 °C
1.2: Reflux
1.3: 0.5 h / 22 °C
2.1: sodium hydroxide / water; tetrahydrofuran / 3 °C
2.2: 1 h / 3 - 22 °C / pH 6 - 7
3.1: N-ethyl-N,N-diisopropylamine / toluene / 50 °C
4.1: toluene-4-sulfonic acid / toluene; methanol / 0 °C
5.1: sodium hydrogencarbonate; acetic acid; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / acetonitrile; water / 0.25 h / 22 - 40 °C
5.2: 0.25 h / 22 °C / pH 6.5 - 7
With
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; hydrogen bromide; sodium hydrogencarbonate; toluene-4-sulfonic acid; acetic acid; N-ethyl-N,N-diisopropylamine; sodium hydroxide;
In
tetrahydrofuran; methanol; dichloromethane; water; toluene; acetonitrile;