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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl phosphorus dichlorideHCID 12573—
ReactantTetrafluoroboric acidHCID 28118—
ReactantLithium BromideHCID 82050—
ReactantHCID 178418310HCID 178418310—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductDI-TERT-BUTYLPHENYLPHOSPHONIUM TETRAFLUOROBORATEHCID 11220595—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230136B2
Source datasetuspto-grants-2007_06
ORD IDord-e126642d23634c8b8d88881e73d569eb
Source noteuspto-grants-2007_06