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[(2R,4S,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-((E)-(3S,4R)-5-ethylsulfanylcarbonyl-4-hydroxy-1,3,5-trimethyl-hex-1-enyl)-2-methoxy-tetrahydro-pyran-2-yl]-acetic acid ethyl ester

Base Information Edit
  • Chemical Name:[(2R,4S,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-((E)-(3S,4R)-5-ethylsulfanylcarbonyl-4-hydroxy-1,3,5-trimethyl-hex-1-enyl)-2-methoxy-tetrahydro-pyran-2-yl]-acetic acid ethyl ester
  • CAS No.:172268-53-0
  • Molecular Formula:C38H56O7SSi
  • Molecular Weight:685.01
  • Hs Code.:
  • Mol file:172268-53-0.mol
[(2R,4S,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-((E)-(3S,4R)-5-ethylsulfanylcarbonyl-4-hydroxy-1,3,5-trimethyl-hex-1-enyl)-2-methoxy-tetrahydro-pyran-2-yl]-acetic acid ethyl ester

Synonyms:[(2R,4S,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-((E)-(3S,4R)-5-ethylsulfanylcarbonyl-4-hydroxy-1,3,5-trimethyl-hex-1-enyl)-2-methoxy-tetrahydro-pyran-2-yl]-acetic acid ethyl ester

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Chemical Property of [(2R,4S,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-((E)-(3S,4R)-5-ethylsulfanylcarbonyl-4-hydroxy-1,3,5-trimethyl-hex-1-enyl)-2-methoxy-tetrahydro-pyran-2-yl]-acetic acid ethyl ester Edit
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Technology Process of [(2R,4S,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-((E)-(3S,4R)-5-ethylsulfanylcarbonyl-4-hydroxy-1,3,5-trimethyl-hex-1-enyl)-2-methoxy-tetrahydro-pyran-2-yl]-acetic acid ethyl ester

There total 16 articles about [(2R,4S,6S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-((E)-(3S,4R)-5-ethylsulfanylcarbonyl-4-hydroxy-1,3,5-trimethyl-hex-1-enyl)-2-methoxy-tetrahydro-pyran-2-yl]-acetic acid ethyl ester 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:
Multi-step reaction with 12 steps
1: 96 percent / tetrahydrofuran; hexane / 0.25 h / -78 °C
2: 83 percent / dicyclohexylcarbodiimide, dimethyl sulfoxide, trifluoroacetic acid, pyridine / benzene / 2 h / Ambient temperature
3: 80 percent / magnesium chloride / tetrahydrofuran; diethyl ether / 1.) reflux 20 min, 2.) -78 deg C, 1.5 h
4: 95 percent / H2, quinoline / 5percent palladium on calcium carbonate / hexane / 1.5 h
5: 1.) potassium hydride, 18-crown-6, 2.) n-butyllithium / 1.) THF, room temperature, 45 min, 2.) THF, hexane, -78 deg C, 1.5 h
6: 74 percent / p-toluenesulfonic acid / dimethylformamide; H2O / 24 h / Heating
7: 90 percent / diisopropylethylamine, 4-(dimethylamino)pyridine / CH2Cl2 / 0.67 h / 0 °C
8: 96 percent / silver carbonate on Celite / benzene / 19 h / Heating
9: 87 percent / LDA / tetrahydrofuran; hexane / 1 h / -78 °C
10: 94 percent / citric acid / 1.5 h / Heating
11: 88 percent / Dess-Martin periodinane / CH2Cl2 / 2.67 h / Ambient temperature
12: 62 percent / LDA / tetrahydrofuran; hexane / 1 h / -78 °C
With pyridine; quinoline; dmap; n-butyllithium; 18-crown-6 ether; hydrogen; potassium hydride; Dess-Martin periodane; toluene-4-sulfonic acid; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; silver carbonate; trifluoroacetic acid; citric acid; magnesium chloride; lithium diisopropyl amide; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; water; N,N-dimethyl-formamide; benzene;
DOI:10.1021/ja972497r
Guidance literature:
Multi-step reaction with 11 steps
1: 83 percent / dicyclohexylcarbodiimide, dimethyl sulfoxide, trifluoroacetic acid, pyridine / benzene / 2 h / Ambient temperature
2: 80 percent / magnesium chloride / tetrahydrofuran; diethyl ether / 1.) reflux 20 min, 2.) -78 deg C, 1.5 h
3: 95 percent / H2, quinoline / 5percent palladium on calcium carbonate / hexane / 1.5 h
4: 1.) potassium hydride, 18-crown-6, 2.) n-butyllithium / 1.) THF, room temperature, 45 min, 2.) THF, hexane, -78 deg C, 1.5 h
5: 74 percent / p-toluenesulfonic acid / dimethylformamide; H2O / 24 h / Heating
6: 90 percent / diisopropylethylamine, 4-(dimethylamino)pyridine / CH2Cl2 / 0.67 h / 0 °C
7: 96 percent / silver carbonate on Celite / benzene / 19 h / Heating
8: 87 percent / LDA / tetrahydrofuran; hexane / 1 h / -78 °C
9: 94 percent / citric acid / 1.5 h / Heating
10: 88 percent / Dess-Martin periodinane / CH2Cl2 / 2.67 h / Ambient temperature
11: 62 percent / LDA / tetrahydrofuran; hexane / 1 h / -78 °C
With pyridine; quinoline; dmap; n-butyllithium; 18-crown-6 ether; hydrogen; potassium hydride; Dess-Martin periodane; toluene-4-sulfonic acid; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; silver carbonate; trifluoroacetic acid; citric acid; magnesium chloride; lithium diisopropyl amide; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; water; N,N-dimethyl-formamide; benzene;
DOI:10.1021/ja972497r
Guidance literature:
Multi-step reaction with 9 steps
1: 95 percent / H2, quinoline / 5percent palladium on calcium carbonate / hexane / 1.5 h
2: 1.) potassium hydride, 18-crown-6, 2.) n-butyllithium / 1.) THF, room temperature, 45 min, 2.) THF, hexane, -78 deg C, 1.5 h
3: 74 percent / p-toluenesulfonic acid / dimethylformamide; H2O / 24 h / Heating
4: 90 percent / diisopropylethylamine, 4-(dimethylamino)pyridine / CH2Cl2 / 0.67 h / 0 °C
5: 96 percent / silver carbonate on Celite / benzene / 19 h / Heating
6: 87 percent / LDA / tetrahydrofuran; hexane / 1 h / -78 °C
7: 94 percent / citric acid / 1.5 h / Heating
8: 88 percent / Dess-Martin periodinane / CH2Cl2 / 2.67 h / Ambient temperature
9: 62 percent / LDA / tetrahydrofuran; hexane / 1 h / -78 °C
With quinoline; dmap; n-butyllithium; 18-crown-6 ether; hydrogen; potassium hydride; Dess-Martin periodane; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; silver carbonate; citric acid; lithium diisopropyl amide; palladium on activated charcoal; In tetrahydrofuran; hexane; dichloromethane; water; N,N-dimethyl-formamide; benzene;
DOI:10.1021/ja972497r
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