HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophosgene → 2-Tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 6-Amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole | HCID 19794186 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole | HCID 15610362 | — |
Reaction Steps
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°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246927 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-6cc07c4d63d84829877b5eb5f5957d9d |
| Source note | uspto-grants-1993_09 |