Réaction #58950

Équation de réaction

2-(4-nitrophenyl)ethanethioamide

2-chloro-cyclohexanone

→

2-(4-nitrobenzyl)-4,5,6,7-tetrahydro-1,3-benzothiazole

Rendement 67.2%

Solvants

tert-butanol

Conditions de réaction

Traitement

1. 1
   Températurewas heated
2. 2
   Températureunder reflux for 3 days
3. 3
   ConcentrationThe reaction mixture was concentrated
4. 4
   workup.ADDITIONsaturated aqueous sodium hydrogen carbonate was added to the residue
5. 5
   ExtractionThe mixture was extracted with ethyl acetate
6. 6
   LavageThe organic layer was washed with saturated brine
7. 7
   Séchagedried over anhydrous magnesium sulfate
8. 8
   Concentrationconcentrated

Mode opératoire

A mixture of 2-(4-nitrophenyl)ethanethioamide (7.0 g), 2-chloro-cyclohexanone (7.28 g) and tert-butanol (100 mL) was heated under reflux for 3 days. The reaction mixture was concentrated, and saturated aqueous sodium hydrogen carbonate was added to the residue. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 2-(4-nitrobenzyl)-4,5,6,7-tetrahydro-1,3-benzothiazole as pale-brown crystals (6.58 g, yield 66%) from a fraction eluted with hexane-ethyl acetate (3:1, v/v). Recrystallization thereof from ethyl acetate-hexane gave pale-yellow prism crystals. melting point: 118-119° C.

Source