(2R,3S,4R,5S,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenylsulfanyl-tetrahydro-pyran-3,4-diol

Base Information

Chemical Name:(2R,3S,4R,5S,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenylsulfanyl-tetrahydro-pyran-3,4-diol
CAS No.:214483-40-6
Molecular Formula:C₁₈H₃₀O₄SSi
Molecular Weight:370.585
Hs Code.:

Synonyms:(2R,3S,4R,5S,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenylsulfanyl-tetrahydro-pyran-3,4-diol

Suppliers and Price of (2R,3S,4R,5S,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenylsulfanyl-tetrahydro-pyran-3,4-diol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (2R,3S,4R,5S,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenylsulfanyl-tetrahydro-pyran-3,4-diol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R,3S,4R,5S,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenylsulfanyl-tetrahydro-pyran-3,4-diol

There total 11 articles about (2R,3S,4R,5S,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenylsulfanyl-tetrahydro-pyran-3,4-diol 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:

Reference yield: 100.0%

: 306768-21-8
Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-5-(tert-butyl-dimethyl-silanyloxy)-6-methyl-2-phenylsulfanyl-tetrahydro-pyran-4-yl ester

: 214483-40-6
(2R,3S,4R,5S,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenylsulfanyl-tetrahydro-pyran-3,4-diol

Guidance literature:: With methanol; potassium carbonate; In tert-butyl alcohol; at 25 ℃; for 3h;
DOI:10.1002/(SICI)1521-3773(19980803)37:13/14<1874::AID-ANIE1874>3.0.CO;2-K

Reference yield:

: 214483-35-9
tert-Butyl-dimethyl-((S)-(R)-1-oxiranyl-allyloxy)-silane

: 214483-40-6
(2R,3S,4R,5S,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenylsulfanyl-tetrahydro-pyran-3,4-diol

Guidance literature:: Multi-step reaction with 8 steps

1: 91 percent / LiEt₃BH / tetrahydrofuran / 1 h / -40 °C

2: 95 percent / Et₃N; DMAP / CH₂Cl₂ / 0.25 h / 0 °C

3: 90 percent / Grubbs' catalyst / CH₂Cl₂ / 34 h / 35 °C

4: 90 percent / DIBAL / CH₂Cl₂ / 1 h / -78 °C

5: 90 percent / NMO; OsO₄; H₂O / acetone / 12 h / 25 °C

6: 99 percent / Et₃N; DMAP / CH₂Cl₂ / 1 h / 0 - 25 °C

7: 69 percent / BF₃*Et₂O / CH₂Cl₂ / 1 h / -20 °C

8: 97 percent / K₂CO₃; MeOH / diethyl ether / 1 h / 25 °C

With methanol; dmap; osmium(VIII) oxide; N-methyl-2-indolinone; boron trifluoride diethyl etherate; water; diisobutylaluminium hydride; lithium triethylborohydride; potassium carbonate; triethylamine; Grubbs catalyst first generation; In tetrahydrofuran; diethyl ether; dichloromethane; acetone; 1: Reduction / 2: Esterification / 3: Cyclization / 4: Reduction / 5: Addition / 6: Acetylation / 7: Substitution / 8: Deacetylation;
DOI:10.1002/1521-3765(20000901)6:17<3095::AID-CHEM3095>3.0.CO;2-4

Reference yield:

: 214483-36-0
Acrylic acid (1R,2S)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-but-3-enyl ester

: 214483-40-6
(2R,3S,4R,5S,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-2-phenylsulfanyl-tetrahydro-pyran-3,4-diol

Guidance literature:: Multi-step reaction with 6 steps

1: 90 percent / Grubbs' catalyst / CH₂Cl₂ / 34 h / 35 °C

2: 90 percent / DIBAL / CH₂Cl₂ / 1 h / -78 °C

3: 90 percent / NMO; OsO₄; H₂O / acetone / 12 h / 25 °C

4: 99 percent / Et₃N; DMAP / CH₂Cl₂ / 1 h / 0 - 25 °C

5: 69 percent / BF₃*Et₂O / CH₂Cl₂ / 1 h / -20 °C

6: 97 percent / K₂CO₃; MeOH / diethyl ether / 1 h / 25 °C

With methanol; dmap; osmium(VIII) oxide; N-methyl-2-indolinone; boron trifluoride diethyl etherate; water; diisobutylaluminium hydride; potassium carbonate; triethylamine; Grubbs catalyst first generation; In diethyl ether; dichloromethane; acetone; 1: Cyclization / 2: Reduction / 3: Addition / 4: Acetylation / 5: Substitution / 6: Deacetylation;
DOI:10.1002/1521-3765(20000901)6:17<3095::AID-CHEM3095>3.0.CO;2-4