HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 13631104, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Ethyl (2-oxoazetidin-1-yl)acetate | HCID 12680981 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13631104 | HCID 13631104 | — |
Reaction Steps
In 0.8 ml of methanol was dissolved 843 mg of compound (19) and 0.4 ml of conc. ammonia water was added to the solution under ice cooling followed by stirring at room temperature for 18 hours. The reaction mixture was concentrated under reduced pressure. The residue was purified by column chromatography (30 g of silica gel, chloroform-methanol=10:1) to obtain 550 mg of a roughly purified product. The product was treated with a solvent mixture of 3 ml of chloroform and 3 ml of ether to crystallize. Thus 360 mg of α-(2-oxo-1-azetidinyl)acetamide (22) was obtained as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04719207 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-58eab94efa0847459be40573bd5bc63d |
| Source note | uspto-grants-1988_01 |