Methyl (2E,4R,6S,7R)-8-tert-butyldiphenylsilyloxy-4,6-bis(triethylsilyloxy)-7-iodoct-2-enoate

Base Information

Chemical Name:Methyl (2E,4R,6S,7R)-8-tert-butyldiphenylsilyloxy-4,6-bis(triethylsilyloxy)-7-iodoct-2-enoate
CAS No.:261155-73-1
Molecular Formula:C₃₇H₆₁IO₅Si₃
Molecular Weight:797.049
Hs Code.:

Synonyms:Methyl (2E,4R,6S,7R)-8-tert-butyldiphenylsilyloxy-4,6-bis(triethylsilyloxy)-7-iodoct-2-enoate

Suppliers and Price of Methyl (2E,4R,6S,7R)-8-tert-butyldiphenylsilyloxy-4,6-bis(triethylsilyloxy)-7-iodoct-2-enoate

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 Methyl (2E,4R,6S,7R)-8-tert-butyldiphenylsilyloxy-4,6-bis(triethylsilyloxy)-7-iodoct-2-enoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Methyl (2E,4R,6S,7R)-8-tert-butyldiphenylsilyloxy-4,6-bis(triethylsilyloxy)-7-iodoct-2-enoate

There total 6 articles about Methyl (2E,4R,6S,7R)-8-tert-butyldiphenylsilyloxy-4,6-bis(triethylsilyloxy)-7-iodoct-2-enoate 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: 62.0%

: 994-30-9
triethylsilyl chloride

: 223574-25-2
(E)-(4R,6S,7S)-8-(tert-Butyl-diphenyl-silanyloxy)-4,6-dihydroxy-7-iodo-oct-2-enoic acid methyl ester

: 261155-73-1
Methyl (2E,4R,6S,7R)-8-tert-butyldiphenylsilyloxy-4,6-bis(triethylsilyloxy)-7-iodoct-2-enoate

Guidance literature:: With pyridine; at 60 ℃; for 4h;
DOI:10.1039/a904206g

Reference yield:

: 4005-46-3,4494-96-6,22248-87-9,142941-40-0
3-deoxy-1,2-O-isopropylidene-D-glucose

: 261155-73-1
Methyl (2E,4R,6S,7R)-8-tert-butyldiphenylsilyloxy-4,6-bis(triethylsilyloxy)-7-iodoct-2-enoate

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / imidazole / dimethylformamide

2: 96 percent / I₂; PPh₃; imidazole / xylene / 80 °C

3: 86 percent / H₂SO₄; H₂O / tetrahydrofuran; dioxane

4: 75 percent

5: 62 percent / pyridine / 4 h / 60 °C

With pyridine; 1H-imidazole; sulfuric acid; water; iodine; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide; xylene; 1: Etherification / 2: Substitution / 3: Hydrolysis / 4: Condensation / 5: Etherification;
DOI:10.1039/a904206g

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 261155-73-1
Methyl (2E,4R,6S,7R)-8-tert-butyldiphenylsilyloxy-4,6-bis(triethylsilyloxy)-7-iodoct-2-enoate

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / imidazole / dimethylformamide

2: 96 percent / I₂; PPh₃; imidazole / xylene / 80 °C

3: 86 percent / H₂SO₄; H₂O / tetrahydrofuran; dioxane

4: 75 percent

5: 62 percent / pyridine / 4 h / 60 °C

With pyridine; 1H-imidazole; sulfuric acid; water; iodine; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide; xylene; 1: Etherification / 2: Substitution / 3: Hydrolysis / 4: Condensation / 5: Etherification;
DOI:10.1039/a904206g