HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-[4-(Trifluoromethyl)phenoxy]azetidine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Nitrourea | HCID 62372 | — |
| Reactant | 3-[4-(Trifluoromethyl)phenoxy]azetidine | HCID 12812499 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-[4-(Trifluoromethyl)phenoxy]azetidine-1-carboxamide | HCID 13565792 | 55.3% |
Reaction Steps
A solution of 9.6 g (0.025 mole) of 3-(4-trifluoromethylphenoxy)azetidine 56.66% (contains diphenylmethane) in 50 ml of acetone was treated with 4.22 g (0.045 mole) of nitro urea and 5 ml of water. The mixture washeated on a hot plate until a clear solution was obtained then allowed to cool to ambient temperature during the next 4 hr. The reaction was diluted with 200 ml of ice water and an oil separated (diphenylmethane) which was dissolved in 30/60 petroleum ether and separated. Upon standing, a fine white precipitate formed in the aqueous solution. Filtration yielded 3.6 g of fine white crystals, m.p. 176°-178° C. After drying under 0.5 mmHg vacuum at 80° C., the product weight was reduced to 3.1 g, m.p. 178°-179° C.; yield was 47.7%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04571393 |
| Source dataset | uspto-grants-1986_02 |
| ORD ID | ord-b9eb825f1d8d49cda75bd154490e6f04 |
| Source note | uspto-grants-1986_02 |