Technology Process of C8H11IO5
There total 10 articles about C8H11IO5 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
boron trichloride;
In
dichloromethane;
at -78 ℃;
for 1h;
Inert atmosphere;
DOI:10.1021/ja203642n
- Guidance literature:
-
Multi-step reaction with 5 steps
1: toluene-4-sulfonic acid / tetrahydrofuran / 80 °C / Inert atmosphere
2: chloro-trimethyl-silane; sodium cyanoborohydride / acetonitrile / 0 °C / Inert atmosphere; Heating
3: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / ethyl acetate / 3 h / 80 °C / Inert atmosphere
4: magnesium iodide / dichloromethane / -78 - -20 °C / Inert atmosphere
5: boron trichloride / dichloromethane / 1 h / -78 °C / Inert atmosphere
With
chloro-trimethyl-silane; boron trichloride; sodium cyanoborohydride; toluene-4-sulfonic acid; magnesium iodide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;
In
tetrahydrofuran; dichloromethane; ethyl acetate; acetonitrile;
4: intramolecular halo-Michael aldol reaction;
DOI:10.1021/ja203642n
- Guidance literature:
-
Multi-step reaction with 7 steps
1: sodium chlorite; sodium phosphate monobasic monohydrate / 2-methyl-but-2-ene; water; tert-butyl alcohol / 0 °C
2: sulfuric acid / 0 - 20 °C / Inert atmosphere
3: toluene-4-sulfonic acid / tetrahydrofuran / 80 °C / Inert atmosphere
4: chloro-trimethyl-silane; sodium cyanoborohydride / acetonitrile / 0 °C / Inert atmosphere; Heating
5: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / ethyl acetate / 3 h / 80 °C / Inert atmosphere
6: magnesium iodide / dichloromethane / -78 - -20 °C / Inert atmosphere
7: boron trichloride / dichloromethane / 1 h / -78 °C / Inert atmosphere
With
sodium chlorite; chloro-trimethyl-silane; sodium phosphate monobasic monohydrate; sulfuric acid; boron trichloride; sodium cyanoborohydride; toluene-4-sulfonic acid; magnesium iodide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;
In
tetrahydrofuran; 2-methyl-but-2-ene; dichloromethane; water; ethyl acetate; acetonitrile; tert-butyl alcohol;
1: Pinnick oxidation / 6: intramolecular halo-Michael aldol reaction;
DOI:10.1021/ja203642n