HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl isocyanate → N-Ethyl-3-[4-(trifluoromethyl)phenoxy]-1-azetidinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | 3-[4-(Trifluoromethyl)phenoxy]azetidine | HCID 12812499 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | N-Ethyl-3-[4-(trifluoromethyl)phenoxy]-1-azetidinecarboxamide | HCID 19799590 | 42.8% |
Reaction Steps
A solution of 6.5 g (0.03 mole) of crude 3-[4-(trifluoromethyl)phenoxy]azetidine in 50 ml of isopropyl ether was stirred under a blanket of nitrogen while 2.85 g (0.04 mole) of ethyl isocyanate was added dropwise. After stirring for 2 hr at ambient temperature, a solid began to precipitate, and after 4 hr, the solid was collected by filtration to yield 3.7 g of beige product, m.p. 94°-96° C. Rework of the filtrate gave only a trace of additional product. The product was recrystallized from isopropyl ether/hexane (treated with charcoal) to yield 2.61 g (30%) of product, m.p. 109°-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05183902 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-62053d83654f4e7c92e967b7cac2377b |
| Source note | uspto-grants-1993_02 |