HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Phosphine, 1H-inden-1-yldiphenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chlorodiphenylphosphine | HCID 66180 | — |
| Reactant | Lithium, 1H-inden-1-yl- | HCID 11116044 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phosphine, 1H-inden-1-yldiphenyl- | HCID 12074547 | 84% |
Reaction Steps
In the drybox lithium indenide (8.00 g, 65.52 mmol) dissolved in 50 mL of THF was added within 15 minutes to a 180 mL ether solution of diphenylchlorophosphine (14.46 g, 65.52 mmol) (diphenylchlorophosphine was distilled before use (97° C. @ 0.4 torr)). After stirring overnight, LiCl was separated by filtration giving a yellow solution. Solvent was removed under vacuum leaving an off-white solid. This solid was triturated with 40 mL of hexane. Hexane was removed by decanting and the solid was dried under reduced pressure to give 16.43 g of off-white solid. Yield 84 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06268444B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-e5eba6eaea484f278dfc49b2ef32fa2d |
| Source note | uspto-grants-2001_07 |