Technology Process of H-ORN(ALOC)-OH
There total 1 articles about H-ORN(ALOC)-OH which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
L-ornithine hydrochloride;
With
copper (II) carbonate hydroxide;
In
water;
at 100 ℃;
for 1h;
With
sodium carbonate;
In
water;
at 20 ℃;
for 0.333333h;
Allyl chloroformate;
Further stages;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 4 h / 100 °C
2.1: N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline / dichloromethane / 4 h / 20 °C
3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / Reflux
3.2: 5 h / 100 °C
4.1: tetrakis(triphenylphosphine) palladium(0); 1,3-dimethylbarbituric acid / tetrahydrofuran / 16 h / 50 °C / Inert atmosphere
With
tetrakis(triphenylphosphine) palladium(0); 1,3-dimethylbarbituric acid; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; dichloromethane;
- Guidance literature:
-
Multi-step reaction with 2 steps
1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 4 h / 100 °C
2: N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline / dichloromethane / 4 h / 20 °C
With
N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; dichloromethane;
