3,7-anhydro-1,2-dideoxy-8-O-(4-toluenesulfonyl)-D-glycero-D-gulo-oct-1-enitol

Base Information

Chemical Name:3,7-anhydro-1,2-dideoxy-8-O-(4-toluenesulfonyl)-D-glycero-D-gulo-oct-1-enitol
CAS No.:202803-14-3
Molecular Formula:C₁₅H₂₀O₇S
Molecular Weight:344.386
Hs Code.:

Synonyms:3,7-anhydro-1,2-dideoxy-8-O-(4-toluenesulfonyl)-D-glycero-D-gulo-oct-1-enitol

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Chemical Property of 3,7-anhydro-1,2-dideoxy-8-O-(4-toluenesulfonyl)-D-glycero-D-gulo-oct-1-enitol

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Technology Process of 3,7-anhydro-1,2-dideoxy-8-O-(4-toluenesulfonyl)-D-glycero-D-gulo-oct-1-enitol

There total 4 articles about 3,7-anhydro-1,2-dideoxy-8-O-(4-toluenesulfonyl)-D-glycero-D-gulo-oct-1-enitol 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: 62.0%

: 51450-27-2
3,7-anhydro-1,2-dideoxy-D-glycero-D-gulo-oct-1-enitol

: 98-59-9
p-toluenesulfonyl chloride

: 202803-14-3
3,7-anhydro-1,2-dideoxy-8-O-(4-toluenesulfonyl)-D-glycero-D-gulo-oct-1-enitol

Guidance literature:: With pyridine;
DOI:10.1002/anie.199727931

Reference yield:

: 51450-26-1
4,5,6,8-Tetra-O-acetyl-3,7-anhydro-1,2-didesoxy-β-D-gluco-oct-1-enitol

: 202803-14-3
3,7-anhydro-1,2-dideoxy-8-O-(4-toluenesulfonyl)-D-glycero-D-gulo-oct-1-enitol

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / sodium methoxide / methanol / Cooling

2: 49 percent / pyridine / 48 h / 20 °C

With pyridine; sodium methylate; In methanol;
DOI:10.1002/ejoc.200600455

Reference yield:

: 572-09-8
2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide

: 202803-14-3
3,7-anhydro-1,2-dideoxy-8-O-(4-toluenesulfonyl)-D-glycero-D-gulo-oct-1-enitol

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrahydrofuran / 5 h / Heating

1.2: 25 percent / pyridine; Ac₂O / 20 °C

2.1: 86 percent / sodium methoxide / methanol / Cooling

3.1: 49 percent / pyridine / 48 h / 20 °C

With pyridine; sodium methylate; In tetrahydrofuran; methanol; 1.1: Grignard reaction;
DOI:10.1002/ejoc.200600455