HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1,4-dihydro-1-(2-iodoethyl)-4-methyl-5H-tetrazol-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(2-chloroethyl)-1,4-dihydro-5H-tetrazol-5-one | HCID 135829347 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | 1,4-dihydro-1-(2-iodoethyl)-4-methyl-5H-tetrazol-5-one | HCID 13676719 | 85% |
Reaction Steps
A mixture of 49 parts of iodomethane, 10.5 parts of 1-(2-chloroethyl)-1,4-dihydro-5H-tetrazol-5-one, 15 parts of sodium carbonate, 0.2 parts of potassium iodide and 240 parts of 4-methyl-2-pentanone is stirred and refluxed overnight with water-separator. The reaction mixture is cooled, 100 parts of water are added and the layers are separated. The aqueous phase is extracted with dichloromethane. The combined organic phases are dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using trichloromethane as eluent. The pure fractions are collected and the eluent is evaporated, yielding 15 parts (85%) of 1,4-dihydro-1-(2-iodoethyl)-4-methyl-5H-tetrazol-5-one as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04167574 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-ca68393763014a85a584fef82393eec1 |
| Source note | uspto-grants-1979_09 |