Technology Process of ((1S,2S,3S)-1-Butyl-4-hydroxy-2,3-bis-methoxymethoxy-non-8-enyl)-carbamic acid benzyl ester
There total 18 articles about ((1S,2S,3S)-1-Butyl-4-hydroxy-2,3-bis-methoxymethoxy-non-8-enyl)-carbamic acid benzyl ester 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 7 steps
1: 75 percent / 1 M LiBH(sec-Bu)3 / tetrahydrofuran / 1 h / -78 °C
2: 51 percent / triphenyl phosphine, diethyl azodicarboxylate / tetrahydrofuran / 14 h / Ambient temperature
3: 76 percent / H2 / 10percent Pd/C / methanol / 3 h
4: 86 percent / oxalyl chloride, dimethyl sulfoxide / CH2Cl2 / 1 h / -78 °C
5: 1.) Mg / 1.) THF, 2.) THF, -78 deg C, 30 min
6: hydrazine hydrate / ethanol / 2 h / Heating
7: aq. Na2CO3 / CH2Cl2 / 0.08 h / 0 °C
With
oxalyl dichloride; hydrogen; L-Selectride; sodium carbonate; hydrazine hydrate; magnesium; dimethyl sulfoxide; triphenylphosphine; diethylazodicarboxylate;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; ethanol; dichloromethane;
DOI:10.1021/ja00186a038
- Guidance literature:
-
Multi-step reaction with 9 steps
1: 1.) Mg / 1.) Et2O, 2.) Et2O, room temp., 14 h
2: 95 percent / oxalyl chloride, dimethyl sulfoxide / CH2Cl2 / 1 h / -78 °C
3: 75 percent / 1 M LiBH(sec-Bu)3 / tetrahydrofuran / 1 h / -78 °C
4: 51 percent / triphenyl phosphine, diethyl azodicarboxylate / tetrahydrofuran / 14 h / Ambient temperature
5: 76 percent / H2 / 10percent Pd/C / methanol / 3 h
6: 86 percent / oxalyl chloride, dimethyl sulfoxide / CH2Cl2 / 1 h / -78 °C
7: 1.) Mg / 1.) THF, 2.) THF, -78 deg C, 30 min
8: hydrazine hydrate / ethanol / 2 h / Heating
9: aq. Na2CO3 / CH2Cl2 / 0.08 h / 0 °C
With
oxalyl dichloride; hydrogen; L-Selectride; sodium carbonate; hydrazine hydrate; magnesium; dimethyl sulfoxide; triphenylphosphine; diethylazodicarboxylate;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; ethanol; dichloromethane;
DOI:10.1021/ja00186a038
- Guidance literature:
-
Multi-step reaction with 8 steps
1: 95 percent / oxalyl chloride, dimethyl sulfoxide / CH2Cl2 / 1 h / -78 °C
2: 75 percent / 1 M LiBH(sec-Bu)3 / tetrahydrofuran / 1 h / -78 °C
3: 51 percent / triphenyl phosphine, diethyl azodicarboxylate / tetrahydrofuran / 14 h / Ambient temperature
4: 76 percent / H2 / 10percent Pd/C / methanol / 3 h
5: 86 percent / oxalyl chloride, dimethyl sulfoxide / CH2Cl2 / 1 h / -78 °C
6: 1.) Mg / 1.) THF, 2.) THF, -78 deg C, 30 min
7: hydrazine hydrate / ethanol / 2 h / Heating
8: aq. Na2CO3 / CH2Cl2 / 0.08 h / 0 °C
With
oxalyl dichloride; hydrogen; L-Selectride; sodium carbonate; hydrazine hydrate; magnesium; dimethyl sulfoxide; triphenylphosphine; diethylazodicarboxylate;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; ethanol; dichloromethane;
DOI:10.1021/ja00186a038