HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → 3-Fluoro-4-(2,2,2-trifluoroethoxy)benzyl isothiocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 14774192 | HCID 14774192 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Fluoro-4-(2,2,2-trifluoroethoxy)benzyl isothiocyanate | HCID 14774193 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
The crude 3-fluoro-4-(2,2,2-trifluoroethoxy)benzylamine (7.54 g) was added dropwise to a mixture of 7.45 g of DCC, 15 ml of carbon disulfide and 30 ml of diethyl ether with stirring at -10° C. The temperature of the mixture was returned to room temperature, and it was left to stand for 3 hours. The reaction mixture was filtered, and the residue was washed with ethyl ether and combined with the filtrate. The solvent was evaporated under reduced pressure. The resulting oily product was purified by column chromatography (silica gel; developing
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05021412 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-47dcedfaae6a43fb805a229d95f388a5 |
| Source note | uspto-grants-1991_06 |