4-nitrophenyl O-(2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranosyl)-(1->6)-2-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranoside

Base Information

Chemical Name:4-nitrophenyl O-(2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranosyl)-(1->6)-2-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranoside
CAS No.:142329-91-7
Molecular Formula:C₃₃H₄₀N₂O₁₄
Molecular Weight:688.686
Hs Code.:

Synonyms:4-nitrophenyl O-(2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranosyl)-(1->6)-2-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranoside

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Chemical Property of 4-nitrophenyl O-(2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranosyl)-(1->6)-2-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranoside

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Technology Process of 4-nitrophenyl O-(2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranosyl)-(1->6)-2-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranoside

There total 4 articles about 4-nitrophenyl O-(2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranosyl)-(1->6)-2-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranoside 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: 88.0%

: 98-88-4
benzoyl chloride

: 142329-90-6
4-nitrophenyl O-(2-acetamido-2-deoxy-4,6-O-isopopylidene-β-D-glucopyranosyl)-(1->6)-3,4-O-isopropylidene-β-D-galactopyranoside

: 142329-91-7
4-nitrophenyl O-(2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranosyl)-(1->6)-2-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranoside

Guidance literature:: With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane; for 1h; Ambient temperature;
DOI:10.1016/S0008-6215(00)90562-7

Reference yield:

: 64970-92-9
4-nitrophenyl 3,4-O-isopropylidene-β-D-galactopyranoside

: 142329-91-7
4-nitrophenyl O-(2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranosyl)-(1->6)-2-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 41.5 percent / 4-toluenesulfonic acid monohydrate / 1,2-dichloro-ethane / 16 h / 70 °C

2: 1.) 0.01 M sodium methoxide, methanol, 2.) 4-toluenesulfonic acid monohydrate / 1.) r.t., 3 h, 2.) DMF, r.t., 16 h

3: 88 percent / 5 percent aq. NaOH, tetrabutylammonium hydrogen sulfate / CH₂Cl₂ / 1 h / Ambient temperature

With methanol; sodium hydroxide; p-toluenesulfonic acid monohydrate; sodium methylate; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane; 1,2-dichloro-ethane;
DOI:10.1016/S0008-6215(00)90562-7

Reference yield:

: 142329-89-3
4-nitrophenyl O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopranosyl)-(1->6)-3,4-isopropylidene-β-D-galactopyranoside

: 142329-91-7
4-nitrophenyl O-(2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranosyl)-(1->6)-2-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) 0.01 M sodium methoxide, methanol, 2.) 4-toluenesulfonic acid monohydrate / 1.) r.t., 3 h, 2.) DMF, r.t., 16 h

2: 88 percent / 5 percent aq. NaOH, tetrabutylammonium hydrogen sulfate / CH₂Cl₂ / 1 h / Ambient temperature

With methanol; sodium hydroxide; p-toluenesulfonic acid monohydrate; sodium methylate; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane;
DOI:10.1016/S0008-6215(00)90562-7