Technology Process of 3,4-Octanedione,
2-(2-ethyl-1,3-dioxolan-2-yl)-2-methyl-1-(phenylmethoxy)-, (2R)-
There total 12 articles about 3,4-Octanedione,
2-(2-ethyl-1,3-dioxolan-2-yl)-2-methyl-1-(phenylmethoxy)-, (2R)- 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
dimethyl sulfoxide; triethylamine; trifluoroacetic anhydride;
In
dichloromethane;
at -78 ℃;
for 0.833333h;
DOI:10.1016/S0040-4039(00)00937-0
- Guidance literature:
-
Multi-step reaction with 8 steps
1: NaHMDS / tetrahydrofuran / -78 °C
2: 85 percent / LiAlH4 / tetrahydrofuran / 1.17 h / 0 °C
3: DMSO; (COCl)2; Et3N / CH2Cl2 / -78 °C
4: Mg / tetrahydrofuran / 0.58 h / -45 °C
5: PCC; MS-4A; NaOAc / CH2Cl2 / 0.5 h / 20 °C
6: 86 percent / BF3*OEt2 / CH2Cl2 / 2 h / 0 °C
7: osmium tertoxide; NMO / acetone; 2-methyl-propan-2-ol; H2O / 120 h
8: TFAA; DMSO; Et3N / CH2Cl2 / 0.83 h / -78 °C
With
osmium(VIII) oxide; lithium aluminium tetrahydride; N-methyl-2-indolinone; oxalyl dichloride; boron trifluoride diethyl etherate; sodium acetate; sodium hexamethyldisilazane; magnesium; dimethyl sulfoxide; triethylamine; pyridinium chlorochromate; trifluoroacetic anhydride;
In
tetrahydrofuran; dichloromethane; water; acetone; tert-butyl alcohol;
1: Alkylation / 2: Reduction / 3: Oxidation / 4: Grignard reaction / 5: Oxidation / 6: Etherification / 7: Oxidation / 8: Oxidation;
DOI:10.1016/S0040-4039(00)00937-0
- Guidance literature:
-
Multi-step reaction with 10 steps
1: 93 percent / SOCl2 / benzene / 3 h / Heating
2: 96 percent / n-BuLi / tetrahydrofuran / -78 °C
3: NaHMDS / tetrahydrofuran / -78 °C
4: 85 percent / LiAlH4 / tetrahydrofuran / 1.17 h / 0 °C
5: DMSO; (COCl)2; Et3N / CH2Cl2 / -78 °C
6: Mg / tetrahydrofuran / 0.58 h / -45 °C
7: PCC; MS-4A; NaOAc / CH2Cl2 / 0.5 h / 20 °C
8: 86 percent / BF3*OEt2 / CH2Cl2 / 2 h / 0 °C
9: osmium tertoxide; NMO / acetone; 2-methyl-propan-2-ol; H2O / 120 h
10: TFAA; DMSO; Et3N / CH2Cl2 / 0.83 h / -78 °C
With
osmium(VIII) oxide; lithium aluminium tetrahydride; n-butyllithium; thionyl chloride; N-methyl-2-indolinone; oxalyl dichloride; boron trifluoride diethyl etherate; sodium acetate; sodium hexamethyldisilazane; magnesium; dimethyl sulfoxide; triethylamine; pyridinium chlorochromate; trifluoroacetic anhydride;
In
tetrahydrofuran; dichloromethane; water; acetone; tert-butyl alcohol; benzene;
1: Chlorination / 2: Acylation / 3: Alkylation / 4: Reduction / 5: Oxidation / 6: Grignard reaction / 7: Oxidation / 8: Etherification / 9: Oxidation / 10: Oxidation;
DOI:10.1016/S0040-4039(00)00937-0