5-O-acetyl-3-O-benzoyl-6-deoxy-6-iodo-1,2-O-isopropylidene-D-allofuranose

Base Information

Chemical Name:5-O-acetyl-3-O-benzoyl-6-deoxy-6-iodo-1,2-O-isopropylidene-D-allofuranose
CAS No.:934339-33-0
Molecular Formula:C₁₈H₂₁IO₇
Molecular Weight:476.265
Hs Code.:

Synonyms:5-O-acetyl-3-O-benzoyl-6-deoxy-6-iodo-1,2-O-isopropylidene-D-allofuranose

Suppliers and Price of 5-O-acetyl-3-O-benzoyl-6-deoxy-6-iodo-1,2-O-isopropylidene-D-allofuranose

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 5-O-acetyl-3-O-benzoyl-6-deoxy-6-iodo-1,2-O-isopropylidene-D-allofuranose

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 5-O-acetyl-3-O-benzoyl-6-deoxy-6-iodo-1,2-O-isopropylidene-D-allofuranose

There total 7 articles about 5-O-acetyl-3-O-benzoyl-6-deoxy-6-iodo-1,2-O-isopropylidene-D-allofuranose 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: 92.0%

: 108-24-7
acetic anhydride

: 143504-31-8
3-O-Benzoyl-6-deoxy-6-iodo-1,2-O-isopropylidene-α-D-allofuranose

: 934339-33-0
5-O-acetyl-3-O-benzoyl-6-deoxy-6-iodo-1,2-O-isopropylidene-D-allofuranose

Guidance literature:: With pyridine; at 20 ℃; for 5h;
DOI:10.1002/ejoc.200600562

Reference yield:

: 2847-00-9
1,2:5,6-di-O-isopropylidene-α-D-hexofuran-3-ulose

: 934339-33-0
5-O-acetyl-3-O-benzoyl-6-deoxy-6-iodo-1,2-O-isopropylidene-D-allofuranose

Guidance literature:: Multi-step reaction with 6 steps

1: 8.0 g / NaBH₄ / ethanol / 0.5 h / 0 °C

2: 90 percent / pyridine / 20 h / 20 °C

3: 91 percent / aq, AcOH / 0.75 h / 60 °C

4: N,N-dimethylaminopyridine / pyridine / 0 - 20 °C

5: 2.88 g / NaI / acetone / Heating

6: 92 percent / pyridine / 5 h / 20 °C

With pyridine; dmap; sodium tetrahydroborate; acetic acid; sodium iodide; In pyridine; ethanol; acetone;
DOI:10.1002/ejoc.200600562

Reference yield:

: 29474-73-5
(+)-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranos-3-yl benzoate

: 934339-33-0
5-O-acetyl-3-O-benzoyl-6-deoxy-6-iodo-1,2-O-isopropylidene-D-allofuranose

Guidance literature:: Multi-step reaction with 4 steps

1: 91 percent / aq, AcOH / 0.75 h / 60 °C

2: N,N-dimethylaminopyridine / pyridine / 0 - 20 °C

3: 2.88 g / NaI / acetone / Heating

4: 92 percent / pyridine / 5 h / 20 °C

With pyridine; dmap; acetic acid; sodium iodide; In pyridine; acetone;
DOI:10.1002/ejoc.200600562