Products Categories
CAS No.: | 62555-05-9 |
---|---|
Name: | Silane, [[1-(3-iodo-2-propenyl)-1-methylpentyl]oxy]trimethyl-, (E)- |
Article Data: | 10 |
Molecular Structure: | |
Formula: | C12H25IOSi |
Molecular Weight: | 340.32 |
Synonyms: | [[1-(3-iodo-2(E)-propenyl)-1-methylpentyl]oxy]trimethylsilane;dl-(E)-4-methyl-4-trimethylsilyloxy-1-iodo-1-octene;(+/-)-(E)-1-iodo-4-methyl-4-trimethylsilyloxy-1-octene;4-trimethylsilyloxy-4-methyl-l-iodo-l-octene;1-Iodo-4-methyl-4-trimethylsilyloxy-trans-1-octene;(dl)-(E)-4-methyl-4-trimethylsilyloxy-1-iodo-1-octene; |
PSA: | 9.23000 |
LogP: | 5.12560 |
4-methyl-4-trimethylsilyloxyl-1-octyne
(1E)-(4R)-4-trimethylsilyloxy-4-methyl-1-iodo-1octene
Conditions | Yield |
---|---|
With N-iodo-succinimide; Schwartz's reagent 1.) THF, RT, 20 min, 2.) RT; Multistep reaction; | |
With Schwartz's reagent; iodine 1) THF, 25 deg C, 30 min, 2) 0 deg C, 10 min, THF; Yield given. Multistep reaction; |
1H-imidazole
1-iodo-4-hydroxy-4-methyl-trans-1-octene
(1E)-(4R)-4-trimethylsilyloxy-4-methyl-1-iodo-1octene
Conditions | Yield |
---|---|
With chloro-trimethyl-silane In N-methyl-acetamide; hexane | |
With chloro-trimethyl-silane In N-methyl-acetamide; hexane | |
With chloro-trimethyl-silane In N-methyl-acetamide; hexane | |
With chloro-trimethyl-silane In N-methyl-acetamide; hexane |
1H-imidazole
1-iodo-4-hydroxy-4-methyl-trans-octene
(1E)-(4R)-4-trimethylsilyloxy-4-methyl-1-iodo-1octene
Conditions | Yield |
---|---|
With chloro-trimethyl-silane In N-methyl-acetamide; hexane |
2-methyl-but-2-ene
(1E)-(4R)-4-trimethylsilyloxy-4-methyl-1-iodo-1octene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium hydroxide; sodium borohydrid; iodine / tetrahydrofuran 2: chloro-trimethyl-silane / N-methyl-acetamide; hexane View Scheme |
4-[(tert-butyldimethylsilyl)oxy]cyclopent-2-enone
(1E)-(4R)-4-trimethylsilyloxy-4-methyl-1-iodo-1octene
Methyl 6-nitro-6-heptenoate
7-[(1S,2S,3S)-3-(tert-Butyl-dimethyl-silanyloxy)-2-((E)-4-methyl-4-trimethylsilanyloxy-oct-1-enyl)-5-oxo-cyclopentyl]-6-nitro-heptanoic acid methyl ester
Conditions | Yield |
---|---|
With copper(l) iodide; tributylphosphine; tert.-butyl lithium Yield given. Multistep reaction; |
(1E)-(4R)-4-trimethylsilyloxy-4-methyl-1-iodo-1octene
methyl 7-(5-oxo-3-[(triethylsilyl)-oxy]-1-cyclopenten-1-yl)-heptanoate
7-[(1R,2R,3R)-2-((E)-4-Methyl-4-trimethylsilanyloxy-oct-1-enyl)-5-oxo-3-triethylsilanyloxy-cyclopentyl]-heptanoic acid methyl ester
Conditions | Yield |
---|---|
With n-butyllithium; methyllithium 1.) THF, -78 deg C, 1 h, 2.) -78 deg C; Yield given. Multistep reaction; |
(1E)-(4R)-4-trimethylsilyloxy-4-methyl-1-iodo-1octene
(+/-)-methyl 7-<3-<(triethylsilyl)oxy>-5-oxo-1-cyclopenten-1-yl>-4(Z)-heptenoate
(Z)-7-[(1R,2R,3R)-2-((E)-4-Methyl-4-trimethylsilanyloxy-oct-1-enyl)-5-oxo-3-triethylsilanyloxy-cyclopentyl]-hept-4-enoic acid methyl ester
Conditions | Yield |
---|---|
With n-butyllithium; methyllithium 1.) THF, -78 deg C, 1 h, 2.) -78 deg C; Yield given. Multistep reaction; |
(1E)-(4R)-4-trimethylsilyloxy-4-methyl-1-iodo-1octene
(+/-)-methyl 7-<3-<(triethylsilyl)oxy>-5-oxo-1-cyclopenten-1-yl>-4(Z)-heptenoate
Enisoprost
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |