HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isocyanate → N-Methyl 3-phenoxy-1-azetidinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methanesulfonate | HCID 85257 | — |
| Reactant | 3-Phenoxyazetidine | HCID 12812501 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-Methyl 3-phenoxy-1-azetidinecarboxamide | HCID 13420164 | — |
Reaction Steps
The methanesulfonate of 3-phenoxyazetidine (10.5 g., 0.043 mole) was partitioned between 50 ml of benzene and 25 ml. of dilute sodium hydroxide. The benzene layer was dried over calcium sulfate and filtered. The filtrate was treated with 2.6 g. (0.043 mole) of methylisocyanate and the solution was stirred at room temperature for 18 hours. The resulting mixture was concentrated at reduced pressure and the residue was crystallized from a mixture of ethyl acetate-isopropyl ether to give 1.2 g. (14%) of product (m.p. 139°-141° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226861 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-2ea87a6f475d4ea68b6f25720e31af84 |
| Source note | uspto-grants-1980_10 |