2-<(R)-1-benzyloxy>ethylfuranne

Base Information

Chemical Name:2-<(R)-1-benzyloxy>ethylfuranne
CAS No.:74652-76-9
Molecular Formula:C₁₃H₁₄O₂
Molecular Weight:202.253
Hs Code.:

Synonyms:

Suppliers and Price of 2-<(R)-1-benzyloxy>ethylfuranne

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 2-<(R)-1-benzyloxy>ethylfuranne

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-<(R)-1-benzyloxy>ethylfuranne

There total 5 articles about 2-<(R)-1-benzyloxy>ethylfuranne 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:

: 63225-18-3
methyl 2-O-benzoyl-5-O-benzyl-3,6-dideoxy-α-D-arabino-hexofuranoside

: 74652-76-9
2-<(R)-1-benzyloxy>ethylfuranne

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / 4 percent potassium hydroxyde / methanol / Ambient temperature

2: 90 percent / pyridine / Ambient temperature

3: sodium azide / hexamethylphosphoric acid triamide / 60 h / 80 °C

4: silice / CH₂Cl₂

With potassium hydroxide; sodium azide; silica gel; In pyridine; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;
DOI:10.1016/S0008-6215(00)85654-2

Reference yield:

: 6154-71-8
methyl 3,6-dideoxy-α-D-arabino-hexopyranoside

: 74652-76-9
2-<(R)-1-benzyloxy>ethylfuranne

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / aluminium chloride / dioxane / 0.5 h / Ambient temperature

2: 95 percent / 4 percent potassium hydroxyde / methanol / Ambient temperature

3: 90 percent / pyridine / Ambient temperature

4: sodium azide / hexamethylphosphoric acid triamide / 60 h / 80 °C

5: silice / CH₂Cl₂

With potassium hydroxide; aluminium trichloride; sodium azide; silica gel; In 1,4-dioxane; pyridine; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;
DOI:10.1016/S0008-6215(00)85654-2

Reference yield:

: 100-52-7
benzaldehyde

: 74652-76-9
2-<(R)-1-benzyloxy>ethylfuranne

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / aluminium chloride / dioxane / 0.5 h / Ambient temperature

2: 95 percent / 4 percent potassium hydroxyde / methanol / Ambient temperature

3: 90 percent / pyridine / Ambient temperature

4: sodium azide / hexamethylphosphoric acid triamide / 60 h / 80 °C

5: silice / CH₂Cl₂

With potassium hydroxide; aluminium trichloride; sodium azide; silica gel; In 1,4-dioxane; pyridine; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;
DOI:10.1016/S0008-6215(00)85654-2