HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → Bis(2,4,6-trimethylbenzoyl)-4-methylphenylphosphine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2,4,6-Trimethylbenzoyl chloride | HCID 97038 | — |
| Reactant | 4-Tolylphosphine | HCID 4379937 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Bis(2,4,6-trimethylbenzoyl)-4-methylphenylphosphine | HCID 22623559 | — |
Reaction Steps
A solution of 16.2 g of diisopropylamine in 50 ml of tetrahydrofuran (THF) is cooled to −10° C. 100 ml of butyllithium in hexane (1.6 M) are added dropwise. Then, at −40° C., first 9.0 g of 4-methylphenylphosphine and, subsequently, a solution of 29.22 g of 2,4,6-trimethylbenzoyl chloride in 150 ml of THF are added. The solution is stirred for 1.5 hours and then the solvent is removed under reduced pressure, to give 28.0 g of bis(2,4,6-trimethylbenzoyl)-4-methylphenylphosphine as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06361925B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-e0590c9930ad47cd96cada60fe576e9c |
| Source note | uspto-grants-2002_03 |