Technology Process of 2,4,6,8-Nonatetraenoic acid,9-(2-ethyl-6,6-dimethyl-1-cyclohexen- 1-yl)-3,7-dimethyl-,ethyl ester,(2E,4E,6E,8E)-
There total 6 articles about 2,4,6,8-Nonatetraenoic acid,9-(2-ethyl-6,6-dimethyl-1-cyclohexen- 1-yl)-3,7-dimethyl-,ethyl ester,(2E,4E,6E,8E)- which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
potassium tert-butylate;
In
tetrahydrofuran; tert-butyl alcohol;
at 55 ℃;
for 16h;
DOI:10.1021/jm00183a010
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 1.) LDA / 1.) THF, Et2O, hexane, 2.) THF, Et2O, hexane, -15 deg C, 3.5 h
2: oxalic acid / H2O; tetrahydrofuran; diethyl ether; hexane / 15 h / Ambient temperature
4: PBr3, pyridine / hexane; diethyl ether / 1.75 h / -5 - 0 °C
5: CH2Cl2 / 68 h / Ambient temperature
6: 48 percent / KO-t-BU / 2-methyl-propan-2-ol; tetrahydrofuran / 16 h / 55 °C
With
pyridine; potassium tert-butylate; oxalic acid; phosphorus tribromide; lithium diisopropyl amide;
In
tetrahydrofuran; diethyl ether; hexane; dichloromethane; water; tert-butyl alcohol;
DOI:10.1021/jm00183a010
- Guidance literature:
-
Multi-step reaction with 8 steps
1: 1.) LDA / 1.) THF, 0 deg C, 40 min, 2.) THF, -78 deg C, 1 h
2: 1.) MeI, 2.) 0.1 N aq. NaHCO3 / 1.) aq. EtOH, reflux, 4.25 h, 2.) benzene, RT, overnight
3: 1.) LDA / 1.) THF, Et2O, hexane, 2.) THF, Et2O, hexane, -15 deg C, 3.5 h
4: oxalic acid / H2O; tetrahydrofuran; diethyl ether; hexane / 15 h / Ambient temperature
6: PBr3, pyridine / hexane; diethyl ether / 1.75 h / -5 - 0 °C
7: CH2Cl2 / 68 h / Ambient temperature
8: 48 percent / KO-t-BU / 2-methyl-propan-2-ol; tetrahydrofuran / 16 h / 55 °C
With
pyridine; potassium tert-butylate; oxalic acid; phosphorus tribromide; sodium hydrogencarbonate; lithium diisopropyl amide; methyl iodide;
In
tetrahydrofuran; diethyl ether; hexane; dichloromethane; water; tert-butyl alcohol;
DOI:10.1021/jm00183a010