Technology Process of 3-Cyclohexen-1-ol, 3-(10-hydroxy-7-methyl-3,7-decadienyl)-4-methyl-,
(E,E)-
There total 25 articles about 3-Cyclohexen-1-ol, 3-(10-hydroxy-7-methyl-3,7-decadienyl)-4-methyl-,
(E,E)- 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 9 steps
1: 93 percent / PBr3 / diethyl ether / 0 °C
2: 1) Na, 2) 1.1 M KOH / 2) 18-cronw-6 / 1) EtOH, r.t., 2) EtOH, r.t. to reflux
3: 100 percent / 10percent aq. NaOH / Heating
4: 76 percent / Li, EtNH2 / 10 h / -78 °C
5: 53 percent / imidazole / dimethylformamide / Ambient temperature
6: 66 percent / LiAlH4 / tetrahydrofuran / Ambient temperature
7: 89 percent / Collins reagent
8: 80 percent / PhLi / tetrahydrofuran; diethyl ether / -78 - -30 °C
9: 1) nBu4NF, 2) Li, NH3 / 1) THF, r.t., 2) THF, -40 deg C
With
1H-imidazole; potassium hydroxide; sodium hydroxide; lithium aluminium tetrahydride; Collins oxidation agent; tetrabutyl ammonium fluoride; ammonia; sodium; phosphorus tribromide; lithium; ethylamine; phenyllithium;
2) 18-cronw-6;
In
tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1039/c39840000721
- Guidance literature:
-
Multi-step reaction with 14 steps
1: 93 percent / NaH / tetrahydrofuran / Heating
2: 75 percent / 2 M aq. H2SO4 / acetone / Heating
3: 98 percent / HCl / ethanol / Heating
4: 85 percent / diethyl ether / Ambient temperature
5: DBU / tetrahydrofuran / 4 h / -5 °C
6: diethyl ether / -78 °C
7: 62 percent / Hg(OAc)2 / Heating
8: Claisen rearrangement
9: 92 percent / LiAlH4 / tetrahydrofuran
10: 85 percent / pyridine / 0 °C
11: 88 percent / NaI / acetone / Ambient temperature
12: 84 percent / benzene / 84 °C
13: 80 percent / PhLi / tetrahydrofuran; diethyl ether / -78 - -30 °C
14: 1) nBu4NF, 2) Li, NH3 / 1) THF, r.t., 2) THF, -40 deg C
With
hydrogenchloride; lithium aluminium tetrahydride; sulfuric acid; mercury(II) diacetate; tetrabutyl ammonium fluoride; ammonia; lithium; sodium hydride; phenyllithium; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium iodide;
In
tetrahydrofuran; pyridine; diethyl ether; ethanol; acetone; benzene;
DOI:10.1039/c39840000721
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 91 percent / imidazole / dimethylformamide / 16 h / 42 °C
2: 66 percent / NBS, H2O / tetrahydrofuran / 3 h / 5 °C
3: 90 percent / K2CO3 / methanol
4: 88 percent / HIO4 / diethyl ether / 0.5 h / Ambient temperature
5: 80 percent / PhLi / tetrahydrofuran; diethyl ether / -78 - -30 °C
6: 1) nBu4NF, 2) Li, NH3 / 1) THF, r.t., 2) THF, -40 deg C
With
1H-imidazole; N-Bromosuccinimide; tetrabutyl ammonium fluoride; ammonia; water; lithium; potassium carbonate; phenyllithium; periodic acid;
In
tetrahydrofuran; methanol; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1039/c39840000721