HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 15171054, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | HCID 86743921 | HCID 86743921 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15171054 | HCID 15171054 | 75% |
Reaction Steps
7.0 g (0.02 mol) of 2,2-dimethylpropionyl chloride 2,6-dichloro-4-trifluoromethylphenylhydrazone and 1.7 g (0.04 mol) of cyanamide were added to 100 ml of tetrahydrofuran. Then, 4.0 g (0.04 mol) of triethylamine was dropwise added under reflux and stirring. After completion of the dropwise addition, the stirring was continued at the same temperature for further 1 hour. After cooling, the reaction solution was poured into water, and the precipitate was extracted with toluene. The organic layer was washed with water and dried. Then, the solvent was distilled off under reduced pressure, and the residue was washed with n-hexane to obtain 5.3 g (yield: 74.6%) of the desired compound as white prismatic crystals. The melting point: 208°-212° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04925864 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-f5b3b22fbe1d4a4fb252e9dc61efb124 |
| Source note | uspto-grants-1990_05 |