HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Triphenylphosphoranylidene)acetone → HCID 23035652, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Triphenylphosphoranylidene)acetone | HCID 15038 | — |
| Reactant | 1,4-Diphenylazetidine-2,3-dione | HCID 13360086 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 23035652 | HCID 23035652 | — |
Reaction Steps
To a solution of 0.67 g of acetylmethylene triphenylphosphorane in 70 ml of benzene was added at room temperature under a nitrogen atmosphere a solution of 0.50 g of 1,4-diphenyl-2,3-azetidinedione in 30 ml of benzene, and the mixture was stirred overnight. After completion of the reaction, the benzene was evaporated, and the residue was applied to silica gel column chromatography (eluent; methylene chloride). The desired fractions were combined, the solvent was evaporated, and the residue was recrystallized from ethanol to give the title compound as pale yellow needles. Yield 0.32 g, m.p. 157.5°-158.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04803266 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-49b56e971ba74661bab039432acaa0e9 |
| Source note | uspto-grants-1989_02 |