Technology Process of 5,8,11-Trioxa-2-azadocosanoic acid, 22-mercapto-,
11-[ethoxy(4-nitrophenoxy)phosphinyl]undecyl ester
There total 8 articles about 5,8,11-Trioxa-2-azadocosanoic acid, 22-mercapto-,
11-[ethoxy(4-nitrophenoxy)phosphinyl]undecyl ester which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
triethylamine; diothiothreitol;
In
methanol;
at 20 ℃;
for 20h;
Inert atmosphere;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: Fusarium solani pisi cutinase; water; propyl-phosphonic acid ethyl ester-(4-nitro-phenyl ester) / aq. phosphate buffer; dimethyl sulfoxide / 20 °C / pH 7 / Inert atmosphere; Enzymatic reaction
2.1: oxalyl dichloride / dichloromethane / 8 h / 0 - 20 °C / Inert atmosphere
2.2: 10 h / 20 °C / Inert atmosphere
3.1: triethylamine / N,N-dimethyl-formamide / 66 h / 60 °C / Inert atmosphere
4.1: triethylamine; diothiothreitol / methanol / 20 h / 20 °C / Inert atmosphere
With
oxalyl dichloride; propyl-phosphonic acid ethyl ester-(4-nitro-phenyl ester); water; triethylamine; diothiothreitol; Fusarium solani pisi cutinase;
In
methanol; aq. phosphate buffer; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: oxalyl dichloride / dichloromethane / 8 h / 0 - 20 °C / Inert atmosphere
1.2: 10 h / 20 °C / Inert atmosphere
2.1: triethylamine / N,N-dimethyl-formamide / 66 h / 60 °C / Inert atmosphere
3.1: triethylamine; diothiothreitol / methanol / 20 h / 20 °C / Inert atmosphere
With
oxalyl dichloride; triethylamine; diothiothreitol;
In
methanol; dichloromethane; N,N-dimethyl-formamide;