HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766696Generated: November 1, 2026
Phenyl phosphorus dichloride → DI-TERT-BUTYLPHENYLPHOSPHONIUM TETRAFLUOROBORATE
https://huagongshe.com/reaction/1766696
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl phosphorus dichloride | HCID 12573 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | HCID 178418310 | HCID 178418310 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | DI-TERT-BUTYLPHENYLPHOSPHONIUM TETRAFLUOROBORATE | HCID 11220595 | — |
Reaction Steps
In a round-bottomed flask, 60.6 mg of copper(I)bromide-dimethyl sulphide complex and 51.2 mg of lithium bromide are initially charged under protective gas. 20 ml of hexane, 4 ml of dichlorophenylphosphine and another 19 ml of hexane are subsequently added. The reaction solution is cooled to 0° C. 32.4 ml of a 2 M solution of tert-butylmagnesium chloride in ether are then slowly added dropwise. The mixture is subsequently allowed to slowly adjust to room temperature and is then stirred at room temperature for a further two hours. For workup, the mixture is cautiously admixed with 75 ml of degassed 2 M HBF4. Another 5 ml of 8 M HBF4 are then additionally added and stirred for 15 min. Filtration with suction is then effected and the filter cake is washed with a little cold water. The residue is dried under reduced pressure to constant weight. Yield: 7.9 g (86% of theory) purity >99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07230136B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-e126642d23634c8b8d88881e73d569eb |
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| Source note | uspto-grants-2007_06 |
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