methyl (phenyl 4,7,8-tri-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate

Base Information

Chemical Name:methyl (phenyl 4,7,8-tri-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate
CAS No.:243866-51-5
Molecular Formula:C₅₆H₅₄O₈S
Molecular Weight:887.106
Hs Code.:

Synonyms:methyl (phenyl 4,7,8-tri-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate

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Chemical Property of methyl (phenyl 4,7,8-tri-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate

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Technology Process of methyl (phenyl 4,7,8-tri-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate

There total 1 articles about methyl (phenyl 4,7,8-tri-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate 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: 71.0%

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

: 100-39-0
benzyl bromide

: 243866-50-4
methyl (phenyl 9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate

: 243866-51-5
methyl (phenyl 4,7,8-tri-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate

: 243866-52-6
methyl (phenyl 4,5,7,8-tetra-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate

Guidance literature:: benzyl bromide; methyl (phenyl 9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate; With barium hydroxide octahydrate; barium(II) oxide; In N,N-dimethyl-formamide; at 20 ℃; for 28h;

diazomethane; In methanol; at 20 ℃; for 1h;
DOI:10.1080/07328309908544026

Reference yield: 93.0%

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

: 100-39-0
benzyl bromide

: 243866-51-5
methyl (phenyl 4,7,8-tri-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate

: 243866-52-6
methyl (phenyl 4,5,7,8-tetra-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate

Guidance literature:: benzyl bromide; methyl (phenyl 4,7,8-tri-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate; With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃; for 28h;

diazomethane; In methanol; at 20 ℃; for 1h;
DOI:10.1080/07328309908544026

Reference yield:

: 243866-51-5
methyl (phenyl 4,7,8-tri-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate

: methyl (phenyl 4,5,7,8-tetra-O-benzyl-3-deoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / dimethylformamide / 28 h / 20 °C

1.2: 93 percent / methanol / 1 h / 20 °C

2.1: 91 percent / Dowex 50W-X₈ (H⁺ form) / methanol; CHCl₃ / 12 h / Heating

With Dowex 50W-X₈ (H⁺ form); sodium hydride; In methanol; chloroform; N,N-dimethyl-formamide; 1.1: Alkylation / 1.2: Methylation / 2.1: detritylation;
DOI:10.1080/07328309908544026