HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-methylpentan-2-one → 4-Hydroxy-4-isobutyl-3-(6-methylpyrid-2-yl)-thiazolidine-2-thione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-methylpentan-2-one | HCID 13720928 | — |
| Reactant | Triethylammonium 6-methylpyrid-2-yldithiocarbamate | HCID 20393055 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Hydroxy-4-isobutyl-3-(6-methylpyrid-2-yl)-thiazolidine-2-thione | HCID 20393072 | 59.8% |
Reaction Steps
The procedure of Example 4 is followed but starting with triethylammonium (6-methylpyrid-2-yl)dithiocarbamate (28.5 g) and 1-chloro-4-methylpentan-2-one (13.4 g) in anhydrous acetonitrile (200 cc) at a temperature between 20 and 25° C. The reaction is continued for 2 hours at 20°-25° C. After recrystallisation of the product from diisopropyl ether (390 cc) and filtration of the boiling solution, there is obtained 4-hydroxy-4-isobutyl-3-(6-methylpyrid-2-yl)-thiazolidine-2-thione (16.8 g) melting at 95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04164579 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-c5e6fa6238bd46d1acdb559987495305 |
| Source note | uspto-grants-1979_08 |