3-C-(2,3,6-tri-O-benzyl-α-D-xylo-hex-4-ulopyranosyl)propene

Base Information

Chemical Name:3-C-(2,3,6-tri-O-benzyl-α-D-xylo-hex-4-ulopyranosyl)propene
CAS No.:800393-85-5
Molecular Formula:C₃₀H₃₂O₅
Molecular Weight:472.581
Hs Code.:

Synonyms:3-C-(2,3,6-tri-O-benzyl-α-D-xylo-hex-4-ulopyranosyl)propene

Suppliers and Price of 3-C-(2,3,6-tri-O-benzyl-α-D-xylo-hex-4-ulopyranosyl)propene

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 3-C-(2,3,6-tri-O-benzyl-α-D-xylo-hex-4-ulopyranosyl)propene

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3-C-(2,3,6-tri-O-benzyl-α-D-xylo-hex-4-ulopyranosyl)propene

There total 4 articles about 3-C-(2,3,6-tri-O-benzyl-α-D-xylo-hex-4-ulopyranosyl)propene 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:

: 1125-88-8
benzaldehyde dimethyl acetal

: 800393-85-5
3-C-(2,3,6-tri-O-benzyl-α-D-xylo-hex-4-ulopyranosyl)propene

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaOMe / methanol / 4 h / 20 °C

1.2: 74 percent / p-TsOH / acetonitrile / 20 °C

2.1: 71 percent / NaH / dimethylformamide

3.1: 88 percent / 3 Angstroem molecular sieves; NaCNBH₃; HCl / tetrahydrofuran; diethyl ether / 2 h / 0 °C

4.1: 90 percent / 4 Angstroem molecular sieves; NaOAc; PCC / CH₂Cl₂ / 3 h / 20 °C

With hydrogenchloride; 3 A molecular sieve; 4 A molecular sieve; sodium methylate; sodium acetate; sodium hydride; sodium cyanoborohydride; pyridinium chlorochromate; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.carres.2004.08.008

Reference yield:

: 53263-18-6,82659-53-8,98920-46-8,98920-48-0,98920-49-1,103773-87-1,98920-44-6
allyl 2,3,4,6-tetra-O-acetyl-α-D-galactopyranoside

: 800393-85-5
3-C-(2,3,6-tri-O-benzyl-α-D-xylo-hex-4-ulopyranosyl)propene

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaOMe / methanol / 4 h / 20 °C

1.2: 74 percent / p-TsOH / acetonitrile / 20 °C

2.1: 71 percent / NaH / dimethylformamide

3.1: 88 percent / 3 Angstroem molecular sieves; NaCNBH₃; HCl / tetrahydrofuran; diethyl ether / 2 h / 0 °C

4.1: 90 percent / 4 Angstroem molecular sieves; NaOAc; PCC / CH₂Cl₂ / 3 h / 20 °C

With hydrogenchloride; 3 A molecular sieve; 4 A molecular sieve; sodium methylate; sodium acetate; sodium hydride; sodium cyanoborohydride; pyridinium chlorochromate; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.carres.2004.08.008

Reference yield:

: 800393-83-3
3-C-(4,6-O-benzylidene-α-D-galactopyranosyl)propene

: 800393-85-5
3-C-(2,3,6-tri-O-benzyl-α-D-xylo-hex-4-ulopyranosyl)propene

Guidance literature:: Multi-step reaction with 3 steps

1: 71 percent / NaH / dimethylformamide

2: 88 percent / 3 Angstroem molecular sieves; NaCNBH₃; HCl / tetrahydrofuran; diethyl ether / 2 h / 0 °C

3: 90 percent / 4 Angstroem molecular sieves; NaOAc; PCC / CH₂Cl₂ / 3 h / 20 °C

With hydrogenchloride; 3 A molecular sieve; 4 A molecular sieve; sodium acetate; sodium hydride; sodium cyanoborohydride; pyridinium chlorochromate; In tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.carres.2004.08.008