Technology Process of 2,2-Dimethyl-thiopropionic acid S-(2-{1-[(Z)-4-(tert-butyl-diphenyl-silanyloxymethyl)-3-hydroxy-7-trimethylsilanyl-hept-4-ene-1,6-diynyl]-cyclopropyl}-ethyl) ester
There total 11 articles about 2,2-Dimethyl-thiopropionic acid S-(2-{1-[(Z)-4-(tert-butyl-diphenyl-silanyloxymethyl)-3-hydroxy-7-trimethylsilanyl-hept-4-ene-1,6-diynyl]-cyclopropyl}-ethyl) ester which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 95 percent / 4-(dimethylamino)pyridine, triethylamine / tetrahydrofuran / 3.5 h / 23 °C
2: 1.) tert-butyllithium / 1.) THF, Et2O, pentane, -120 deg C, 2.) THF, Et2O, pentane, from -120 to -40 deg C, 3 h
3: 1.) lithium diisopropylamide, Cerium(III) chloride / 1.) THF, -78 deg C, 30 min, 2.) THF, -78 deg C, 40 min
With
dmap; cerium(III) chloride; tert.-butyl lithium; triethylamine; lithium diisopropyl amide;
In
tetrahydrofuran;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 94 percent / diisobutylaluminum hydride / hexane; toluene / a) -78 deg C, 30 min, b) 0 deg C, 30 min
2: 95 percent / 4-(dimethylamino)pyridine, triethylamine / tetrahydrofuran / 3.5 h / 23 °C
3: 1.) tert-butyllithium / 1.) THF, Et2O, pentane, -120 deg C, 2.) THF, Et2O, pentane, from -120 to -40 deg C, 3 h
4: 1.) lithium diisopropylamide, Cerium(III) chloride / 1.) THF, -78 deg C, 30 min, 2.) THF, -78 deg C, 40 min
With
dmap; cerium(III) chloride; tert.-butyl lithium; diisobutylaluminium hydride; triethylamine; lithium diisopropyl amide;
In
tetrahydrofuran; hexane; toluene;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: triethylamine / CH2Cl2 / 0.08 h / 0 °C
2: 90 percent / triethylamine / tetrahydrofuran / 3 h / 50 °C
3: 1.) lithium diisopropylamide, Cerium(III) chloride / 1.) THF, -78 deg C, 30 min, 2.) THF, -78 deg C, 40 min
With
cerium(III) chloride; triethylamine; lithium diisopropyl amide;
In
tetrahydrofuran; dichloromethane;