octyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->4)-3-O-allyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Base Information

Chemical Name:octyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->4)-3-O-allyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
CAS No.:503602-46-8
Molecular Formula:C₆₆H₇₅NO₁₂
Molecular Weight:1074.32
Hs Code.:

Synonyms:octyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->4)-3-O-allyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

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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 octyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->4)-3-O-allyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

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Technology Process of octyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->4)-3-O-allyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

There total 5 articles about octyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->4)-3-O-allyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 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: 35.0%

: 100-39-0
benzyl bromide

: 503602-45-7
octyl 3,4,6-tri-O-benzyl-β-D-galactopyranosyl-(1->4)-3-O-allyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

: 503602-46-8
octyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->4)-3-O-allyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: With tetra-(n-butyl)ammonium iodide; sodium hydride; In N,N-dimethyl-formamide; at 0 ℃;
DOI:10.1016/S0008-6215(02)00178-7

Reference yield:

: 161664-93-3
octyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

: 503602-46-8
octyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->4)-3-O-allyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 56 percent / sodium hydride / dimethylformamide / 3 h / 20 °C

2: 96 percent / sodium cyanoborohydride; HCl; 4A molecular sieves / tetrahydrofuran; diethyl ether / 0 - 20 °C

3: 80 percent / N-iodosuccinimide; 4A molecular sieves / CH₂Cl₂ / 0 °C

4: 77 percent / sodium / methanol / 48 h / 20 °C

5: 35 percent / tetrabutylammonium iodide; NaH / dimethylformamide / 0 °C

With hydrogenchloride; N-iodo-succinimide; 4 A molecular sieve; sodium; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium cyanoborohydride; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(02)00178-7

Reference yield:

: 503602-15-1
octyl 3-O-allyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

: 503602-46-8
octyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->4)-3-O-allyl-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 96 percent / sodium cyanoborohydride; HCl; 4A molecular sieves / tetrahydrofuran; diethyl ether / 0 - 20 °C

2: 80 percent / N-iodosuccinimide; 4A molecular sieves / CH₂Cl₂ / 0 °C

3: 77 percent / sodium / methanol / 48 h / 20 °C

4: 35 percent / tetrabutylammonium iodide; NaH / dimethylformamide / 0 °C

With hydrogenchloride; N-iodo-succinimide; 4 A molecular sieve; sodium; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium cyanoborohydride; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(02)00178-7