Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925047Generated: October 30, 2026

Phosphine → HCID 178425658, compound

https://huagongshe.com/reaction/925047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphineHCID 24404—
ReactantChlorodiisopropylphosphineHCID 538967—
ReactantHCID 67297609HCID 67297609—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 178425658HCID 17842565889%

Reaction Conditions

Temperature0 °C

Reaction Steps

N2-(2-isopropylphenyl)-4-methylbenzamidine (1.26 g, 5.0 mmol) was dissolved in 25 mL of diethylether and cooled to 0° C. Butyllithium (2.50 mL of 2.0 M solution in pentane, 5.0 mmol) was added dropwise, producing a fluffy white suspended solid. The slurry was warmed to room temperature and stirred for 2 hours. Chlorodiisopropylphosphine (0.80 mL, 5.0 mmol) was added slowly at room temperature. The suspended solid became finer and denser and the solution became slightly yellow upon complete addition of the phosphine. Stirring was continued for 1 hour. The solution was filtered to remove a small amount of white solid, presumably lithium chloride, and the solvent was removed in vacuo. The yellow foamy residue was suspended in 25 mL of pentane, stirred for 2 hours and taken to dryness under vacuum, affording 1.64 g (70%) of yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09283555B2
Source datasetuspto-grants-2016_03
ORD IDord-dd1b1856589b4c3bbda201c64247be74
Source noteuspto-grants-2016_03