HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → (1-(4-chloro-2-fluorophenyl)-1H-tetrazol-5-yl)ethyl sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178505829 | HCID 178505829 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (1-(4-chloro-2-fluorophenyl)-1H-tetrazol-5-yl)ethyl sulfide | HCID 14551620 | 81.4% |
Reaction Steps
A solution of 1.75 g (0.0076 mole) of 1-(4-chloro-2-fluorophenyl)-1,4-dihydro-5H-tetrazol-5-thione, 0.57 ml (0.0076 mole) of bromoethane, and 1.6 g (0.012 mole) of potassium carbonate in 8 ml of acetone was stirred at room temperature for seven hours. The solvent was evaporated from the reaction mixture under reduced pressure leaving a residue. This residue was dissolved in diethyl ether and the organic solution was washed with water. The washed organic phase was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to yield 1.6 g of (1-(4-chloro-2-fluorophenyl)-1H-tetrazol-5-yl) ethyl sulfide as a solid, m.p. 76°-79° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04868321 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-a280ca4d37d7426f87e652ddc7c69646 |
| Source note | uspto-grants-1989_09 |