HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 3-(4-Fluorophenoxy)-1-azetidinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-(4-Fluorophenoxy)-1-azetidinecarbonyl chloride | HCID 15053367 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Fluorophenoxy)-1-azetidinecarboxamide | HCID 15053438 | — |
Reaction Steps
A solution of 5.52 g (0.022 mole) of crude 3-(4-fluorophenoxy)-1-azetidine carbonyl chloride in 20 ml of tetrahydrofuran was treated with 10 ml of concentrated ammonium hydroxide while stirring. The exothermic reaction mixture was stirred for 18 hr as it cooled to ambient temperature. The reaction mixture was diluted with 400 ml of ice water to produce a phase separation. Upon standing, the oily phase solidified and was collected by filtration yielding 12.5 g of crude wet product. Recrystallization from aqueous ethanol after charcoal treatment produced an oil which slowly crystallized. The sample was recrystallized from methylene chloride, yield 1.6 g (35%) of amorphous-like powder, m.p. 185°-188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05151418 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-3733e42aebab425eaa71e925e9bd7b0c |
| Source note | uspto-grants-1992_09 |