phenyl 4-O-benzoyl-3-O-benzyl-2-O-(2-trifluoromethylbenzenesulfonyl)-1-thio-β-L-rhamnopyranoside

Base Information

Chemical Name:phenyl 4-O-benzoyl-3-O-benzyl-2-O-(2-trifluoromethylbenzenesulfonyl)-1-thio-β-L-rhamnopyranoside
CAS No.:503065-97-2
Molecular Formula:C₃₃H₂₉F₃O₇S₂
Molecular Weight:658.716
Hs Code.:

Synonyms:phenyl 4-O-benzoyl-3-O-benzyl-2-O-(2-trifluoromethylbenzenesulfonyl)-1-thio-β-L-rhamnopyranoside

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Chemical Property of phenyl 4-O-benzoyl-3-O-benzyl-2-O-(2-trifluoromethylbenzenesulfonyl)-1-thio-β-L-rhamnopyranoside

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Technology Process of phenyl 4-O-benzoyl-3-O-benzyl-2-O-(2-trifluoromethylbenzenesulfonyl)-1-thio-β-L-rhamnopyranoside

There total 8 articles about phenyl 4-O-benzoyl-3-O-benzyl-2-O-(2-trifluoromethylbenzenesulfonyl)-1-thio-β-L-rhamnopyranoside 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: 88.0%

: 98-88-4
benzoyl chloride

: 503065-95-0
phenyl 3-O-benzyl-2-O-(2-trifluoromethylbenzenesulfonyl)-1-thio-β-L-rhamnopyranoside

: 503065-97-2
phenyl 4-O-benzoyl-3-O-benzyl-2-O-(2-trifluoromethylbenzenesulfonyl)-1-thio-β-L-rhamnopyranoside

Guidance literature:: With dmap; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1021/ol0340890

Reference yield:

: 776-04-5
2-trifluoromethylbenzenesulfonyl chloride

: 503065-97-2
phenyl 4-O-benzoyl-3-O-benzyl-2-O-(2-trifluoromethylbenzenesulfonyl)-1-thio-β-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 52 percent / Ag₂O; KI; collidine / CH₂Cl₂ / 37 h / 0 - 20 °C

2: 88 percent / DMAP / CH₂Cl₂ / 3 h / 20 °C

With 2,3,5-trimethyl-pyridine; dmap; potassium iodide; silver(l) oxide; In dichloromethane;
DOI:10.1021/ol0340890

Reference yield:

: 100-39-0
benzyl bromide

: 503065-97-2
phenyl 4-O-benzoyl-3-O-benzyl-2-O-(2-trifluoromethylbenzenesulfonyl)-1-thio-β-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1.1: Bu₂SnO / benzene / 4 h / Heating

1.2: 71 percent / CsF / dimethylformamide / 18 h / 20 °C

2.1: 52 percent / Ag₂O; KI; collidine / CH₂Cl₂ / 37 h / 0 - 20 °C

3.1: 88 percent / DMAP / CH₂Cl₂ / 3 h / 20 °C

With 2,3,5-trimethyl-pyridine; dmap; di(n-butyl)tin oxide; potassium iodide; silver(l) oxide; In dichloromethane; benzene;
DOI:10.1021/ol0340890