| Identification | More | [Name]
Benzyltriphenylphosphonium bromide | [CAS]
1449-46-3 | [Synonyms]
BENZYLTRIPHENYLPHOSPHONIUM BROMIDE
BENZYL TRIPHENYL PHOSPHOROUS BROMIDE
TZP
Phosphonium,triphenyl(phenylmethyl)-,bromide
Benzytriphenyl Phosphonium Bromide
benzyl trphenyl phosphonium bromide
Benzyltriphenylphosphanium bromid
Triphenylbenzylphosphonium·bromide | [EINECS(EC#)]
215-908-4 | [Molecular Formula]
C25H22BrP | [MDL Number]
MFCD00031707 | [Molecular Weight]
433.32 | [MOL File]
1449-46-3.mol |
| Questions And Answer | Back Directory | [Preparation]
Benzyl triphenylphosphonium bromide is prepared by the following steps:To a solution of Ph3P (22 g, 0.084 mol) in toluene, BnBr (10 ml, 0.084 mol) was added dropwise with ice-cooling and stirred at room temperature for 2 hours. A solid was formed, which was filtered and washed with toluene and then dry pet ether to remove unreacted Ph3P. The salt was dried under vacuum (35 g, 96% yield). |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [WGK Germany ]
3
| [HazardClass ]
6.1 | [PackingGroup ]
III | [HS Code ]
29319090 |
| Hazard Information | Back Directory | [Chemical Properties]
WHITE CRYSTALLINE POWDER | [Uses]
Benzyltriphenylphosphonium bromide is used as a reactant for stereoselective azidolysis of vinyl epoxides, enantioselective aziridination and Friedel-Crafts cyclization for asymmetric synthesis of dihydrexidine, biomimetic iron(III) mediated oxidative dimerization for synthesis of benzoquinone parvistemin A, enantioselective synthesis of syn-diarylheptanoids from D-glucose, preparation of β-amyloid plaque ligands and decarboxylative cyclopropanation. It react with 4-methyl-oxetan-2-one to produce 4-hydroxy-1-phenyl-1-(triphenyl-l5-phosphanylidene)-pentan-2-one. | [reaction suitability]
reaction type: C-C Bond Formation |
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