Identification | Back Directory | [Name]
O-DIPHENYLPHOSPHINYLHYDROXYLAMINE | [CAS]
72804-96-7 | [Synonyms]
O-DiphenyL phosphinyL diphenylphosphinate aMino diphenylphosphinate (AMinooxy)diphenylphosphineoxid TwoPhenylphosphonichydroxylaMine Diphenylphosphonoyl hydroxylamine (AMinooxy)diphenylphosphine oxide O-DIPHENYLPHOSPHINYLHYDROXYLAMINE O-(diphenylphosphoryl)hydroxylaMine HydroxylaMine, O-(diphenylphosphinyl)- O-(Diphenylphosphinyl)hydroxylamine Phosphinic acid, P,P-diphenyl-, azanyl ester | [Molecular Formula]
C12H14NO2P | [MDL Number]
MFCD03788194 | [MOL File]
72804-96-7.mol | [Molecular Weight]
235.22 |
Chemical Properties | Back Directory | [Melting point ]
>140℃ (decomposition) | [Boiling point ]
368.0±25.0 °C(Predicted) | [density ]
1.25±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
DMSO (Slightly), Methanol (Very Slightly, Sonicated) | [form ]
solid | [pka]
-1.65±0.70(Predicted) | [color ]
white | [InChI]
InChI=1S/C12H12NO2P/c13-15-16(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,13H2 | [InChIKey]
SJECIYLGISUNRO-UHFFFAOYSA-N | [SMILES]
P(C1=CC=CC=C1)(C1=CC=CC=C1)(ON)=O |
Hazard Information | Back Directory | [Chemical Properties]
Light yellow or white powder solid | [Uses]
Efficient reagent for direct conversion of aldehydes to nitriles in the presence of alcohol, ketone, ester, or amine functionality. | [Synthesis Reference(s)]
Tetrahedron Letters, 23, p. 3835, 1982 DOI: 10.1016/S0040-4039(00)87720-5 | [Description]
O-Diphenylphosphinylhydroxylamine (DPPH) is a versatile electrophilic amination reagent that has been used widely for the amination of stable carbanions, Grignard reagents, and π-electron-rich nitrogen heterocycles. Researchers have used DPPH for the aziridination of enones. Compared to other hydroxylamine derivatives typically stored as hydrochloride salts, this activated phosphinyl reagent exhibits good stability and can be stored indefinitely at 0 ℃. This compound in a single step from hydroxylamine hydrochloride and diphenylphosphinic chloride[1]. | [General Description]
O-(Diphenylphosphinyl)hydroxylamine is a general reagent for electrophilic C-amination, which aminates a variety of stable carbanions and Grignard reagents. | [Synthesis]
The general procedure for the synthesis of diphenylphosphinic acid hydroxylamine from diphenylphosphinic acid chloride is as follows: to a 5 L four-necked round-bottomed flask (RBF) equipped with an overhead stirrer and a thermocouple are added sequentially (1) a solution of 60.85 grams (1.52 moles, 2.4 eq.) of NaOH dissolved in 180 mL of water, (2) 110.12 grams (1.58 moles, 2.5 eq.) of hydroxylamine- HCl dissolved in a solution of 180 mL of water, and (3) 180 mL of dioxane. The mixture was cooled to 0°C in an ice/acetone bath. Subsequently, 150 g of ice was added and a solution of diphenylphosphinic chloride (150.0 g, 0.634 mol, 1 eq.) dissolved in 180 mL of dioxane pre-cooled to about 10°C was added all at once. During the reaction the mixture becomes very viscous with the formation of a white precipitate and vigorous stirring is required. The internal temperature of the reaction rises to 22°C. After continued stirring for 5 to 10 minutes, the reaction mixture was diluted with 2.5 L of ice water and filtered through a large 15 cm diameter sintered funnel. The filter cake was drained on a glass stock for 1 hour, after which it was transferred back into 5 L of RBF. The solid was suspended in 500 mL of ice-cold 0.25 N NaOH solution with vigorous stirring for 5 to 10 min, filtered again, and washed twice with ice water, followed by drying on a porous filter overnight. The partially dried product was dried in a vacuum oven (50 °C, 0.1 Torr) for 12 h, after which it was well pulverized using a mortar and pestle grinder. Finally, the product was dried in a vacuum oven for another 16 hours to give 122 g (82% yield) of the target product diphenylphosphinoylhydroxylamine as a white powder. | [References]
[1] J. P. Anselm, J. L. Ferrari. “A New Journal for Organic Synthesis: Organic Preparations and Procedures International.” Journal of Chemical Education 48 5 (1971): 349.
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