Technology Process of C21H23NO5S
There total 8 articles about C21H23NO5S 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:
-
Multi-step reaction with 10 steps
1: sodium hydride / tetrahydrofuran / Reflux
2: ytterbium(III) triflate / benzene / Reflux
3: sodium tris(acetoxy)borohydride; acetic acid / acetonitrile
4: sodium t-butanolate / tetrahydrofuran
5: lithium aluminium tetrahydride / diethyl ether
6: 20% palladium hydroxide on charcoal; hydrogen / methanol
7: potassium carbonate / dichloromethane
8: tributylphosphine / acetonitrile
9: 3-chloro-benzenecarboperoxoic acid / dichloromethane
10: hydrogenchloride / acetone / Reflux
With
hydrogenchloride; lithium aluminium tetrahydride; tributylphosphine; 20% palladium hydroxide on charcoal; hydrogen; sodium tris(acetoxy)borohydride; sodium hydride; potassium carbonate; acetic acid; 3-chloro-benzenecarboperoxoic acid; sodium t-butanolate; ytterbium(III) triflate;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetone; acetonitrile; benzene;
DOI:10.1016/j.bmcl.2011.12.057
- Guidance literature:
-
Multi-step reaction with 6 steps
1: lithium aluminium tetrahydride / diethyl ether
2: 20% palladium hydroxide on charcoal; hydrogen / methanol
3: potassium carbonate / dichloromethane
4: tributylphosphine / acetonitrile
5: 3-chloro-benzenecarboperoxoic acid / dichloromethane
6: hydrogenchloride / acetone / Reflux
With
hydrogenchloride; lithium aluminium tetrahydride; tributylphosphine; 20% palladium hydroxide on charcoal; hydrogen; potassium carbonate; 3-chloro-benzenecarboperoxoic acid;
In
methanol; diethyl ether; dichloromethane; acetone; acetonitrile;
DOI:10.1016/j.bmcl.2011.12.057