5-deoxy-1,2-O-isopropylidene-6-O-triphenylmethyl-α-D-erythro-hex-3-ulofuranose

Base Information

Chemical Name:5-deoxy-1,2-O-isopropylidene-6-O-triphenylmethyl-α-D-erythro-hex-3-ulofuranose
CAS No.:250128-85-9
Molecular Formula:C₂₈H₂₈O₅
Molecular Weight:444.527
Hs Code.:

Synonyms:5-deoxy-1,2-O-isopropylidene-6-O-triphenylmethyl-α-D-erythro-hex-3-ulofuranose

Suppliers and Price of 5-deoxy-1,2-O-isopropylidene-6-O-triphenylmethyl-α-D-erythro-hex-3-ulofuranose

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-deoxy-1,2-O-isopropylidene-6-O-triphenylmethyl-α-D-erythro-hex-3-ulofuranose

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 5-deoxy-1,2-O-isopropylidene-6-O-triphenylmethyl-α-D-erythro-hex-3-ulofuranose

There total 3 articles about 5-deoxy-1,2-O-isopropylidene-6-O-triphenylmethyl-α-D-erythro-hex-3-ulofuranose 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: 68.0%

: 37070-23-8
5-deoxy-1,2-O-isopropylidene-6-O-triphenylmethyl-α-D-xylohexofuranose

: 250128-85-9
5-deoxy-1,2-O-isopropylidene-6-O-triphenylmethyl-α-D-erythro-hex-3-ulofuranose

Guidance literature:: With 3 A molecular sieve; sodium acetate; pyridinium chlorochromate; In dichloromethane; Heating;
DOI:10.1016/S0008-6215(99)00119-6

Reference yield:

: 7057-09-2
1,2-O-isopropylidene-5-deoxy-α-D-glucofuranose

: 250128-85-9
5-deoxy-1,2-O-isopropylidene-6-O-triphenylmethyl-α-D-erythro-hex-3-ulofuranose

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / pyridine / 48 h / 40 - 50 °C

2: 68 percent / pyridinium chlorochromate; molecular sieves (3 Angstroem); sodium acetate / CH₂Cl₂ / Heating

With 3 A molecular sieve; sodium acetate; pyridinium chlorochromate; In pyridine; dichloromethane; 1: tritylation / 2: Oxidation;
DOI:10.1016/S0008-6215(99)00119-6

Reference yield:

: 76-83-5
trityl chloride

: 250128-85-9
5-deoxy-1,2-O-isopropylidene-6-O-triphenylmethyl-α-D-erythro-hex-3-ulofuranose

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / pyridine / 48 h / 40 - 50 °C

2: 68 percent / pyridinium chlorochromate; molecular sieves (3 Angstroem); sodium acetate / CH₂Cl₂ / Heating

With 3 A molecular sieve; sodium acetate; pyridinium chlorochromate; In pyridine; dichloromethane; 1: tritylation / 2: Oxidation;
DOI:10.1016/S0008-6215(99)00119-6