methyl 5-acetamido-4,7-di-O-benzyl-8,9-O-benzylidene-2,3-didehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate

Base Information

Chemical Name:methyl 5-acetamido-4,7-di-O-benzyl-8,9-O-benzylidene-2,3-didehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate
CAS No.:133585-59-8
Molecular Formula:C₃₃H₃₅NO₈
Molecular Weight:573.643
Hs Code.:

Synonyms:methyl 5-acetamido-4,7-di-O-benzyl-8,9-O-benzylidene-2,3-didehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate

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Chemical Property of methyl 5-acetamido-4,7-di-O-benzyl-8,9-O-benzylidene-2,3-didehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate

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Technology Process of methyl 5-acetamido-4,7-di-O-benzyl-8,9-O-benzylidene-2,3-didehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate

There total 3 articles about methyl 5-acetamido-4,7-di-O-benzyl-8,9-O-benzylidene-2,3-didehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate 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:

: 25875-99-4,79026-38-3
methyl 5-acetamido-2,6-anhydro-3,5-dideoxy-D-glycero-D-galacto-non-2-enonate

: 133585-59-8
methyl 5-acetamido-4,7-di-O-benzyl-8,9-O-benzylidene-2,3-didehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / (+/-)-camphorsulfonic acid / dimethylformamide / 3 h / Ambient temperature

2: 1) CaH₂, Bu₄NI, KOH / 1a) THF, DMSO, 0 deg C, 4h, 1b) RT, 16h, 2) ether

With potassium hydroxide; calcium hydride; camphor-10-sulfonic acid; tetra-(n-butyl)ammonium iodide; In N,N-dimethyl-formamide;
DOI:10.1021/jo00032a601

Reference yield:

: 1125-88-8
benzaldehyde dimethyl acetal

: 133585-59-8
methyl 5-acetamido-4,7-di-O-benzyl-8,9-O-benzylidene-2,3-didehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / (+/-)-camphorsulfonic acid / dimethylformamide / 3 h / Ambient temperature

2: 1) CaH₂, Bu₄NI, KOH / 1a) THF, DMSO, 0 deg C, 4h, 1b) RT, 16h, 2) ether

With potassium hydroxide; calcium hydride; camphor-10-sulfonic acid; tetra-(n-butyl)ammonium iodide; In N,N-dimethyl-formamide;
DOI:10.1021/jo00032a601

Reference yield:

: 186581-53-3,908094-01-9,334-88-3
diazomethane

: 100-39-0
benzyl bromide

: 133585-58-7
methyl 5-acetamido-8,9-O-benzylidene-2,3-didehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate

: 133585-59-8
methyl 5-acetamido-4,7-di-O-benzyl-8,9-O-benzylidene-2,3-didehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate

Guidance literature:: With potassium hydroxide; calcium hydride; tetra-(n-butyl)ammonium iodide; Yield given. Multistep reaction; 1a) THF, DMSO, 0 deg C, 4h, 1b) RT, 16h, 2) ether;
DOI:10.1021/jo00032a601