Technology Process of 5-(1,3-dioxo-4,4-dimethyl-5-benzyloxyhept-6-ynyl)-2,2-dimethyl[1,3]dioxane-4,6-dione
There total 11 articles about 5-(1,3-dioxo-4,4-dimethyl-5-benzyloxyhept-6-ynyl)-2,2-dimethyl[1,3]dioxane-4,6-dione which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
dmap; dicyclohexyl-carbodiimide;
In
dichloromethane;
at 20 ℃;
for 16h;
DOI:10.1021/jo0204707
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: 81 percent / 4-dimethylaminopyridine; triethylamine / CH2Cl2 / 16 h / 20 °C
2.1: NaH / tetrahydrofuran / 16 h / 20 °C
3.1: 901 mg / tetrabutylammonium fluoride / tetrahydrofuran / 16 h / 20 °C
4.1: 92 percent / oxalyl chloride; DMSO; triethylamine / CH2Cl2 / 2 h / -78 - 20 °C
5.1: n-BuLi; diisopropylamine / tetrahydrofuran; hexane / 0.67 h / -78 °C
5.2: 98 percent / tetrahydrofuran; hexane / -78 - 20 °C
6.1: 60 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 16 h / 20 °C
7.1: 76 percent / trifluoroacetic acid / CH2Cl2 / 2.5 h / 0 °C
8.1: 86 percent / 4-dimethylaminopyridine; dicyclohexylcarbodiimide / CH2Cl2 / 16 h / 20 °C
With
dmap; n-butyllithium; oxalyl dichloride; tetrabutyl ammonium fluoride; sodium acetate; sodium hydride; dimethyl sulfoxide; triethylamine; diisopropylamine; dicyclohexyl-carbodiimide; pyridinium chlorochromate; trifluoroacetic acid;
In
tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/jo0204707
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: n-BuLi; diisopropylamine / tetrahydrofuran; hexane / 0.67 h / -78 °C
1.2: 98 percent / tetrahydrofuran; hexane / -78 - 20 °C
2.1: 60 percent / pyridinium chlorochromate; sodium acetate / CH2Cl2 / 16 h / 20 °C
3.1: 76 percent / trifluoroacetic acid / CH2Cl2 / 2.5 h / 0 °C
4.1: 86 percent / 4-dimethylaminopyridine; dicyclohexylcarbodiimide / CH2Cl2 / 16 h / 20 °C
With
dmap; n-butyllithium; sodium acetate; diisopropylamine; dicyclohexyl-carbodiimide; pyridinium chlorochromate; trifluoroacetic acid;
In
tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/jo0204707