HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 22107118, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Hydroxyfluorene | HCID 75547 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | HCID 54262066 | HCID 54262066 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22107118 | HCID 22107118 | 89.2% |
Reaction Steps
A mixture of the compound prepared as described in Example 4 (0.462 g), triphenylphosphine (0.864 g), and 2-hydroxyfluorene (0.600 g) in tetrahydrofuran (4.2 ml) was cooled to approximately 1°-2° C., and treated with a solution of diethylazodicarboxylate (0.573 g) in tetrahydrofuran (1.7 ml) over a five minute period. After the addition was complete, the reaction was allowed to warm to room temperature. After about 24 hours, the resulting suspension was filtered, and the insolubles washed with tetrahydrofuran (5 ml) to give 0.526 g of methyl 3-(2-fluorenoxy)-2-pyrrolidone-5-carboxylate. This material was dried in a vacuum oven at 60° C. for approximately 24 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05576323 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-33e7027d96084206b735a9fd298dc557 |
| Source note | uspto-grants-1996_11 |