Réaction #5883
ord-6cc07c4d63d84829877b5eb5f5957d9d
Équation de réaction
thiophosgene
6-amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole
potassium bicarbonate
→
2-tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Températuremaintaining the temperature at 0°-2°
- 2FiltrationThe solid is filtered
- 3Autrethe filtrate is evaporated
- 4AutreThe solid thus obtained
- 5Filtrationfiltered through a silica gel column
- 6AutreThe filtrate is evaporated
Mode opératoire
To a cooled mixture of 2.1 g of 6-amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole and 2.8 g of potassium bicarbonate in 20 ml of chloroform is added dropwise 1.6 g of thiophosgene in 5 ml of chloroform under stirring. The stirring is continued for 2 hours maintaining the temperature at 0°-2° . The solid is filtered and the filtrate is evaporated. The solid thus obtained is dissolved in chloroform and filtered through a silica gel column. The filtrate is evaporated to give 2-tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole, melting at 54°-58°.