(4R,5S,6R)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one

Base Information

Chemical Name:(4R,5S,6R)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one
CAS No.:137765-35-6
Molecular Formula:C₁₅H₁₉IO₄
Molecular Weight:390.218
Hs Code.:

Synonyms:(4R,5S,6R)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one

Suppliers and Price of (4R,5S,6R)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one

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 (4R,5S,6R)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (4R,5S,6R)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one

There total 1 articles about (4R,5S,6R)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one 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:

: 137664-72-3
Carbonic acid (1R,2R)-1-(2-benzyloxy-ethyl)-2-methyl-but-3-enyl ester tert-butyl ester

: 137765-35-6
(4R,5S,6R)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one

: 137664-73-4
(4R,5S,6S)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one

Guidance literature:: With iodine(I) bromide; In dichloromethane; toluene; at -85 - -80 ℃; for 11h; Product distribution; other solvents, other tmperatures; or with I₂; other homoallylic carbonates; stereoselectivity;
DOI:10.1021/jo00066a024

Reference yield: 83.0%

: 137765-35-6
(4R,5S,6R)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one

: 137664-74-5
(3R,4S)-1-Benzyloxy-4-(R)-oxiranyl-pentan-3-ol

Guidance literature:: With potassium carbonate; In methanol; Ambient temperature;
DOI:10.1016/S0040-4039(00)93479-8

Reference yield:

: 137765-35-6
(4R,5S,6R)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one

: 137664-81-4
(S)-Methoxy-phenyl-acetic acid (1S,2S)-3-{2-[(2S,3S,4R)-6-benzyloxy-2,4-bis-(tert-butyl-dimethyl-silanyloxy)-3-methyl-hexyl]-[1,3]dithian-2-yl}-2-(4-methoxy-benzyloxy)-3-methyl-1-vinyl-butyl ester

Guidance literature:: Multi-step reaction with 8 steps

1.1: K₂CO₃; MeOH

2.1: 99 percent / TMEDA / dimethylformamide

3.1: n-BuLi; HMPA / tetrahydrofuran

3.2: 81 percent / DMPU / tetrahydrofuran / -20 °C

4.1: 95 percent / 2,6-lutidine

5.1: 94 percent / DIBAL / CH₂Cl₂ / -78 - 0 °C

6.1: 87 percent / SO₃*pyridine; DMSO; Et₃N / CH₂Cl₂

7.1: tetrahydrofuran / -78 °C

8.1: 93 percent / DCC; DMAP / CH₂Cl₂

With 2,6-dimethylpyridine; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; n-butyllithium; pyridine-SO₃ complex; N,N,N,N,-tetramethylethylenediamine; diisobutylaluminium hydride; potassium carbonate; dimethyl sulfoxide; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 1.1: Cyclization / 2.1: silylation / 3.1: Metallation / 3.2: Addition / 4.1: silylation / 5.1: reductive cleavage / 6.1: Oxidation / 7.1: Grignard reaction / 8.1: Esterification;
DOI:10.1021/ja992134m