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2H-Pyran, tetrahydro-2-[[(3S,7R)-3,7,11-trimethyl-4-(phenylsulfonyl)dodecyl]oxy]-

Base Information Edit
  • Chemical Name:2H-Pyran, tetrahydro-2-[[(3S,7R)-3,7,11-trimethyl-4-(phenylsulfonyl)dodecyl]oxy]-
  • CAS No.:185681-36-1
  • Molecular Formula:C26H44O4S
  • Molecular Weight:452.699
  • Hs Code.:
  • Mol file:185681-36-1.mol
2H-Pyran,
tetrahydro-2-[[(3S,7R)-3,7,11-trimethyl-4-(phenylsulfonyl)dodecyl]oxy]-

Synonyms:

Suppliers and Price of 2H-Pyran, tetrahydro-2-[[(3S,7R)-3,7,11-trimethyl-4-(phenylsulfonyl)dodecyl]oxy]-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 1 raw suppliers
Chemical Property of 2H-Pyran, tetrahydro-2-[[(3S,7R)-3,7,11-trimethyl-4-(phenylsulfonyl)dodecyl]oxy]- Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 2H-Pyran, tetrahydro-2-[[(3S,7R)-3,7,11-trimethyl-4-(phenylsulfonyl)dodecyl]oxy]-

There total 9 articles about 2H-Pyran, tetrahydro-2-[[(3S,7R)-3,7,11-trimethyl-4-(phenylsulfonyl)dodecyl]oxy]- 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:
(3S)-3-methyl-4-phenylsulfonylbutyl tetrahydropyranyl ether; With lithium diisopropyl amide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; at -78 ℃; for 0.5h;
(3R)-3,7-dimethyloctyl iodide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; at -78 - 20 ℃; for 1h;
DOI:10.1248/cpb.48.272
Guidance literature:
Multi-step reaction with 3 steps
1: 92 percent / H2 / 20percent Pd(OH)2/C / ethyl acetate / 760 Torr / Ambient temperature
2: 90 percent / I2, Ph3P, imidazole / acetonitrile / 1.33 h / 0 - 20 °C
3: 1.) LDA, HMPA / 1.) THF, -78 deg C, 30 min, 2.) THF, a) -78 deg C, 30 min, b) 0 deg C, 30 min
With 1H-imidazole; N,N,N,N,N,N-hexamethylphosphoric triamide; hydrogen; iodine; triphenylphosphine; lithium diisopropyl amide; palladium dihydroxide; In ethyl acetate; acetonitrile;
DOI:10.1248/cpb.44.2153
Guidance literature:
Multi-step reaction with 4 steps
1: 80 percent / LiAlH4 / tetrahydrofuran / 0.25 h / 0 °C
2: 92 percent / H2 / 20percent Pd(OH)2/C / ethyl acetate / 760 Torr / Ambient temperature
3: 90 percent / I2, Ph3P, imidazole / acetonitrile / 1.33 h / 0 - 20 °C
4: 1.) LDA, HMPA / 1.) THF, -78 deg C, 30 min, 2.) THF, a) -78 deg C, 30 min, b) 0 deg C, 30 min
With 1H-imidazole; N,N,N,N,N,N-hexamethylphosphoric triamide; lithium aluminium tetrahydride; hydrogen; iodine; triphenylphosphine; lithium diisopropyl amide; palladium dihydroxide; In tetrahydrofuran; ethyl acetate; acetonitrile;
DOI:10.1248/cpb.44.2153
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