Réaction #67889

Équation de réaction

sodium bicarbonate

triethylamine

((1S,2S,3R,4R)-2-(3-(benzyloxy)benzyl)-4-(tert-butyldimethylsilyoxy)-3-((S,E)-3-(tert-butyl dimethylsilyoxy)oct-1-enyl)cyclopentyl)methanol

p-Toluenesulfonic chloride

→

((1S,2S,3R,4R)-2-(3-(benzyloxy)benzyl)-4-(tert-butyldimethylsilyoxy)-3-((S,E)-3-(tert-butyldimethylsilyoxy)oct-1-enyl)cyclopentyl)methyl 4-methylbenzenesulfonate

Rendement 85.0%

Solvants

CH2Cl2

Conditions de réaction

Traitement

1. 1
   Autreseparated
2. 2
   Extractionthe aqueous layer was extracted with 500 ml ethyl acetate
3. 3
   Séchagedried over anhydrous magnesium sulfate
4. 4
   FiltrationThe solid was filtered off
5. 5
   AutreThe solvent was evaporated off under vacuum
6. 6
   AutreThe crude product was purified by chromatography on silica gel using
7. 7
   workup.ADDITIONa mixture of hexane and ethyl acetate as a gradient eluent

Mode opératoire

A solution of ((1S,2S,3R,4R)-2-(3-(benzyloxy)benzyl)-4-(tert-butyldimethylsilyoxy)-3-((S,E)-3-(tert-butyl dimethylsilyoxy)oct-1-enyl)cyclopentyl)methanol (15 g, 0.023 mol) in dry CH2Cl2 (500 ml) was cooled to 0° C. under nitrogen and treated with triethylamine (9.6 ml, 0.068 mol), then with p-Toluenesulfonic chloride (8.77 g, 0.046 mol). The mixture was poured to saturated sodium bicarbonate aqueous and stirred for 30 minutes. The reaction mixture was phase separated and the aqueous layer was extracted with 500 ml ethyl acetate. The organic layers were combined and dried over anhydrous magnesium sulfate. The solid was filtered off. The solvent was evaporated off under vacuum. The crude product was purified by chromatography on silica gel using a mixture of hexane and ethyl acetate as a gradient eluent. Yield: 85%.

Source