HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetone → 2-Propanone, 1-((1-methyl-1H-tetrazol-5-yl)thio)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178482017 | HCID 178482017 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Propanone, 1-((1-methyl-1H-tetrazol-5-yl)thio)- | HCID 3061977 | 48% |
Reaction Steps
1-Methyl-5-mercapto-1,2,3,4-tetrazole (0.01 mol), potassium carbonate (0.015 mol) and α-chloroacetone (0.015 mol) are added to acetone (50 ml) and the mixture is refluxed with stirring for 2 hours. The reaction mixture is concentrated to dryness under reduced pressure and the residue is dissolved in chloroform. Insolubles are filtered off. The filtrate is concentrated under reduced pressure and the residue is purified by silica gel column chromatography [Kieselgel 60, eluant: benzene-ether (10:1)] and the product is recrystallized from methanol-ether to obtain 1-methyl-5-acetylmethylthio-1,2,3,4-tetrazole (yield 48%) as colorless needles, m.p. 31° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04372953 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-251cd1ba05c642a9817e905ef8c3e208 |
| Source note | uspto-grants-1983_02 |