HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-chloro-2-fluorophenyl-1,4-dihydro-5H-tetrazol-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | (1-(4-chloro-2-fluorophenyl)-1H-tetrazol-5-yl)ethyl sulfide | HCID 14551620 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-chloro-2-fluorophenyl-1,4-dihydro-5H-tetrazol-5-one | HCID 135621797 | — |
Reaction Steps
To a stirred solution of 0.12 g (0.0052 mole) of sodium in 16 ml of ethanol was added 1.2 g (0.0046 mole) of (1-(4-chloro-2-fluorophenyl)-1H-tetrazol-5-yl)ethyl sulfide. The resultant solution was heated at reflux for six hours. The reaction mixture was cooled and the solvent was evaporated under reduced pressure leaving a residue. This residue was dissolved in 40 ml of water and the aqueous solution was washed with diethyl ether. The aqueous phase was acidified with concentrated hydrochloric acid forming a precipitate. The precipitate was collected by filtration and dried to yield 0.55 g of 1-(4-chloro-2-fluorophenyl)-1,4-dihydro-5H-tetrazol-5-one as a solid, m.p. 194° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04868321 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-15de671adb30457e943adb52c6c8b5ce |
| Source note | uspto-grants-1989_09 |