Technology Process of ethyl (Z)-4-[(2S,4S,6S)-6-{[(2R,4R,6R)-6-heptyl-2-phenyl-1,3-dioxan-4-yl]methyl}-2-phenyl-1,3-dioxan-4-yl]but-2-enoate
There total 13 articles about ethyl (Z)-4-[(2S,4S,6S)-6-{[(2R,4R,6R)-6-heptyl-2-phenyl-1,3-dioxan-4-yl]methyl}-2-phenyl-1,3-dioxan-4-yl]but-2-enoate 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:
-
ethyl [bis(2,2,2-trifluoroethoxy)phosphinyl]acetate;
With
sodium hydride;
In
tetrahydrofuran; paraffin;
at -78 ℃;
for 1h;
2-[(2R,4R,6R)-6-{[(2R,4R,6R)-6-heptyl-2-phenyl-1,3-dioxan-4-yl]methyl}-2-phenyl-1,3-dioxan-4-yl]acetaldehyde;
In
tetrahydrofuran; paraffin;
at -78 ℃;
for 0.75h;
DOI:10.1002/ejoc.201100888
- Guidance literature:
-
Multi-step reaction with 10 steps
1.1: titanium(IV) isopropylate; (S)-[1,1']-binaphthalenyl-2,2'-diol / toluene / 36 h / -15 °C / Molecular sieve
2.1: ozone / dichloromethane / 0.08 h / -78 °C
2.2: 18 h / 20 °C
3.1: potassium tert-butylate / tetrahydrofuran / 4 h / 0 °C
4.1: magnesium / tetrahydrofuran; ethylene dibromide / 2 h / 20 °C
5.1: lithium aluminium tetrahydride; lithium iodide / 0.5 h / -100 - -40 °C
6.1: 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide / 1,4-dioxane; water / 4 h / 20 °C
7.1: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride / acetonitrile / 0.5 h / 20 °C
7.2: 24 h / 20 °C
8.1: potassium tert-butylate / tetrahydrofuran / 6 h / 4 °C
9.1: diisobutylaluminium hydride / tetrahydrofuran; toluene / 0.5 h / -78 °C / Inert atmosphere
10.1: sodium hydride / tetrahydrofuran; paraffin / 1 h / -78 °C
10.2: 0.75 h / -78 °C
With
2,6-dimethylpyridine; titanium(IV) isopropylate; sodium periodate; osmium(VIII) oxide; lithium aluminium tetrahydride; potassium tert-butylate; (S)-[1,1']-binaphthalenyl-2,2'-diol; sodium hydride; diisobutylaluminium hydride; ozone; magnesium; 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride; lithium iodide;
In
tetrahydrofuran; 1,4-dioxane; dichloromethane; water; ethylene dibromide; toluene; acetonitrile; paraffin;
1.1: Keck allylation / 2.2: Wittig-Horner reaction / 7.1: Wittig-Horner reaction / 7.2: Wittig-Horner reaction / 8.1: Michael condensation / 10.2: Horner-Wittig reaction;
DOI:10.1002/ejoc.201100888
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: lithium aluminium tetrahydride; lithium iodide / 0.5 h / -100 - -40 °C
2.1: 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide / 1,4-dioxane; water / 4 h / 20 °C
3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride / acetonitrile / 0.5 h / 20 °C
3.2: 24 h / 20 °C
4.1: potassium tert-butylate / tetrahydrofuran / 6 h / 4 °C
5.1: diisobutylaluminium hydride / tetrahydrofuran; toluene / 0.5 h / -78 °C / Inert atmosphere
6.1: sodium hydride / tetrahydrofuran; paraffin / 1 h / -78 °C
6.2: 0.75 h / -78 °C
With
2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide; lithium aluminium tetrahydride; potassium tert-butylate; sodium hydride; diisobutylaluminium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride; lithium iodide;
In
tetrahydrofuran; 1,4-dioxane; water; toluene; acetonitrile; paraffin;
3.1: Wittig-Horner reaction / 3.2: Wittig-Horner reaction / 4.1: Michael condensation / 6.2: Horner-Wittig reaction;
DOI:10.1002/ejoc.201100888