HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 54093447, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | HCID 22165696 | HCID 22165696 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54093447 | HCID 54093447 | — |
Reaction Steps
A mixture of 3-(4-chlorophenyl)1-(1,2,4-triazol-1-yl)butan-2-one (0.7g), trimethylsulphoxonium iodide (0.77g), potassium hydroxide (0.38g) and 1,2,4-triazole (0.24g) in tert butyl alcohol (lOml) was heated at reflux for 4h. The reaction mixture was cooled and poured into water, and the aqueous phase was separated and extracted with ethyl acetate. The organic extract was separated, dried and concentrated to dryness under reduced pressure, and the residue was purified by column chromatography on silica using 2% by volume methanol in chloroform as eluent, to give 3 (4 chlorophenyl)-1-(1,2,4-triazol-1-yl)-2(1,2,4-triazol-1-ylmethyl)butan-2-ol mp 60-64° .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04957934 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-5753f2a8384945d8876229da04949a76 |
| Source note | uspto-grants-1990_09 |