Technology Process of benzyl (1R,2R)-2-(benzyloxy)-1,2,3,4-tetrahydronaphthalen-1-ylcarbamate
There total 4 articles about benzyl (1R,2R)-2-(benzyloxy)-1,2,3,4-tetrahydronaphthalen-1-ylcarbamate 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:
-
With
water; sodium sulfite;
In
hexane; ethyl acetate;
at 20 ℃;
for 14h;
optical yield given as %de;
Inert atmosphere;
DOI:10.1021/jo201794k
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: sodium carbonate / hexane / 0.33 h / -40 °C / Inert atmosphere
1.2: 10 h / -40 °C / Inert atmosphere
2.1: water; sodium sulfite / hexane; ethyl acetate / 14 h / 20 °C / Inert atmosphere
With
water; sodium carbonate; sodium sulfite;
In
hexane; ethyl acetate;
DOI:10.1021/jo201794k
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: sodium hydride / tetrahydrofuran; N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere
1.2: 0 - 20 °C / Inert atmosphere
2.1: sodium carbonate / hexane / 0.33 h / -40 °C / Inert atmosphere
2.2: 10 h / -40 °C / Inert atmosphere
3.1: water; sodium sulfite / hexane; ethyl acetate / 14 h / 20 °C / Inert atmosphere
With
water; sodium hydride; sodium carbonate; sodium sulfite;
In
tetrahydrofuran; hexane; ethyl acetate; N,N-dimethyl-formamide; mineral oil;
DOI:10.1021/jo201794k