2-(tetradecyl)hexadecyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-β-D-glucopyranoside

Base Information

Chemical Name:2-(tetradecyl)hexadecyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-β-D-glucopyranoside
CAS No.:470462-15-8
Molecular Formula:C₅₃H₈₉NO₇
Molecular Weight:852.292
Hs Code.:

Synonyms:2-(tetradecyl)hexadecyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-β-D-glucopyranoside

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Chemical Property of 2-(tetradecyl)hexadecyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-β-D-glucopyranoside

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Technology Process of 2-(tetradecyl)hexadecyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-β-D-glucopyranoside

There total 4 articles about 2-(tetradecyl)hexadecyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-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:

: 158847-14-4
2-tetradecylhexadecan-1-ol

: 470462-15-8
2-(tetradecyl)hexadecyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / 4 Angstroem molecular sieves; N-iodosuccinimide; trifluoromethanesulfonic acid / CH₂Cl₂ / 3 h / 20 °C

2: H₂NNH₂*H₂O / ethanol / 10 h / Heating

3: 377 mg / methanol; CH₂Cl₂ / 14 h / 20 °C

With N-iodo-succinimide; trifluorormethanesulfonic acid; 4 A molecular sieve; hydrazine hydrate; In methanol; ethanol; dichloromethane;
DOI:10.1081/CAR-120004336

Reference yield:

: 169962-29-2
Phenyl 4-O-acetyl-6-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-2-phthalimido-1-thio-β-D-glucopyranoside

: 470462-15-8
2-(tetradecyl)hexadecyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / 4 Angstroem molecular sieves; N-iodosuccinimide; trifluoromethanesulfonic acid / CH₂Cl₂ / 3 h / 20 °C

2: H₂NNH₂*H₂O / ethanol / 10 h / Heating

3: 377 mg / methanol; CH₂Cl₂ / 14 h / 20 °C

With N-iodo-succinimide; trifluorormethanesulfonic acid; 4 A molecular sieve; hydrazine hydrate; In methanol; ethanol; dichloromethane;
DOI:10.1081/CAR-120004336

Reference yield:

: 470462-14-7
2-(tetradecyl)hexadecyl 4-O-acetyl-6-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-2-phthalimido-β-D-glucopyranoside

: 470462-15-8
2-(tetradecyl)hexadecyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: H₂NNH₂*H₂O / ethanol / 10 h / Heating

2: 377 mg / methanol; CH₂Cl₂ / 14 h / 20 °C

With hydrazine hydrate; In methanol; ethanol; dichloromethane;
DOI:10.1081/CAR-120004336