(R)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-2-one

Base Information

Chemical Name:(R)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-2-one
CAS No.:506410-39-5
Molecular Formula:C₄₇H₄₉NO₈
Molecular Weight:755.908
Hs Code.:

Synonyms:(R)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-2-one

Suppliers and Price of (R)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-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 (R)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-2-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-2-one

There total 2 articles about (R)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-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: 70.0%

: 40217-17-2,90719-32-7,120574-96-1,102029-44-7
(R)-4-(phenylmethyl)-2-oxazolidinone

: 506410-38-4
3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionic acid

: 506410-39-5
(R)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-2-one

Guidance literature:: 3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionic acid; With pivaloyl chloride; triethylamine; In tetrahydrofuran; at -78 ℃; for 0.25h;

(R)-4-(phenylmethyl)-2-oxazolidinone; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;
DOI:10.1021/jo026758d

Reference yield:

: 181489-22-5
3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propan-1-ol

: 506410-39-5
(R)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: 99 percent / CrO₃; H₂SO₄ / acetone / 1.5 h / 0 - 20 °C

2.1: Et₃N; pivaloyl chloride / tetrahydrofuran / 0.25 h / -78 °C

2.2: 70 percent / BuLi / hexane; tetrahydrofuran / 0.5 h / -78 °C

With chromium(VI) oxide; sulfuric acid; pivaloyl chloride; triethylamine; In tetrahydrofuran; acetone; 1.1: Jones oxidation;
DOI:10.1021/jo026758d

Reference yield:

: 506410-39-5
(R)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-2-one

: 506410-43-1
(R)-4-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)pent-1-ene

Guidance literature:: Multi-step reaction with 4 steps

1: 62 percent / LDA / hexane; tetrahydrofuran / 2 h / -78 - -20 °C

2: 94 percent / LiEt₃BH / tetrahydrofuran / 0.33 h / 0 °C

3: 90 percent / I₂; PPh₃; imidazole / toluene / 0.33 h / 20 °C

4: 96 percent / LiEt₃BH / tetrahydrofuran / 20 °C

With 1H-imidazole; iodine; lithium triethylborohydride; triphenylphosphine; lithium diisopropyl amide; In tetrahydrofuran; hexane; toluene;
DOI:10.1021/jo026758d