Technology Process of (2R,3R)-2,3-dibenzyloxypentanal
There total 5 articles about (2R,3R)-2,3-dibenzyloxypentanal 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 5 steps
1: 1.) BuLi, 2.) LiAlH4, / 1.) hexane, THF, -10 deg C, 2 h, 2.) hexane, THF, -10 deg C, 4 h,
2: 80 percent / W-2 Raney nickel, / ethanol / 6 h / Heating
3: 90 percent / NaH, / tetrahydrofuran / 2 h
4: 50 percent / AlCl3, LiAlH4, / diethyl ether; CH2Cl2 / 6 h / Ambient temperature
5: 90 percent / oxalyl chloride, methylsulfoxide, / CH2Cl2 / 0.25 h / -60 °C
With
lithium aluminium tetrahydride; n-butyllithium; aluminium trichloride; oxalyl dichloride; W-2 Raney nickel; sodium hydride; dimethyl sulfoxide;
In
tetrahydrofuran; diethyl ether; ethanol; dichloromethane;
DOI:10.1016/S0008-6215(00)90117-4
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 90 percent / NaH, / tetrahydrofuran / 2 h
2: 50 percent / AlCl3, LiAlH4, / diethyl ether; CH2Cl2 / 6 h / Ambient temperature
3: 90 percent / oxalyl chloride, methylsulfoxide, / CH2Cl2 / 0.25 h / -60 °C
With
lithium aluminium tetrahydride; aluminium trichloride; oxalyl dichloride; sodium hydride; dimethyl sulfoxide;
In
tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1016/S0008-6215(00)90117-4