HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Allylhydroxylamine → HCID 178460146, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Allylhydroxylamine | HCID 420841 | — |
| Reactant | 5-(1-Benzofuran-2-yl)-2-butanoylcyclohexane-1,3-dione | HCID 20146016 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178460146 | HCID 178460146 | 92% |
Reaction Steps
4.6 parts by weight of 2-butyryl-5-(benzo[b]fur-2-yl)-cyclohexane-1,3-dione, 1.2 parts by weight of allyloxyamine and 30 parts by volume of ethanol were stirred for 12 hours at room temperature. The solvent was distilled off under reduced pressure, the residue was taken up in 50 parts of dichloromethane, the solution was washed twice with water and dried over sodium sulfate, and the solvent was distilled off under reduced pressure. 2-(1-Allyloxyaminobutylidene)-5-(benzo[b]fur-2-yl)-cyclohexane-1,3-dione was obtained as a viscous oil in a yield of 92% (compound no. 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04734121 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-d1ebeb9149504ef4946bd5ab3cdd1910 |
| Source note | uspto-grants-1988_03 |