Propyltriphenylphosphonium bromide
[CAS# 6228-47-3]

Identification

• Classification: Chemical reagent >> Organic reagent >> Phosphorus halide
• Name: Propyltriphenylphosphonium bromide
• Synonyms: n-Propyltriphenylphosphonium bromide
• Molecular Formula: C₂₁H₂₂P^.Br
• Molecular Weight: 385.28
• CAS Registry Number: 6228-47-3
• EC Number: 228-330-2
• SMILES: CCC[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Br-]

Properties

• Melting point: 235-238 ºC (Expl.)
• Water solubility: soluble

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H315-H319-H335
• Precautionary Statements: P261-P305+P351+P338

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Acute toxicity	Acute Tox.	4	H302
Acute toxicity	Acute Tox.	4	H312
Skin irritation	Skin Irrit.	2	H315
Acute toxicity	Acute Tox.	4	H332
Specific target organ toxicity - single exposure	STOT SE	3	H335
Eye irritation	Eye Irrit.	2	H319
Acute toxicity	Acute Tox.	3	H301
Eye irritation	Eye Irrit.	2A	H319
Chronic hazardous to the aquatic environment	Aquatic Chronic	2	H411

Discovory and Applicatios

Propyltriphenylphosphonium bromide, with the molecular formula C21H21BrP, is a quaternary ammonium salt featuring a triphenylphosphonium cation and a propyl group. This compound is typically synthesized by reacting triphenylphosphine with an alkyl halide such as propyl bromide. The resulting salt appears as a white to light yellow crystalline solid that is soluble in organic solvents such as acetone, methanol, and chloroform.

The discovery of propyltriphenylphosphonium bromide is tied to the broader development of phosphonium salts, which have been widely studied due to their utility in organic synthesis. These compounds are particularly useful in the generation of reactive intermediates, such as ylides, which play a crucial role in a number of synthetic transformations.

One of the primary applications of propyltriphenylphosphonium bromide is in the Wittig reaction, a method used to synthesize alkenes from carbonyl compounds. In this reaction, the phosphonium salt undergoes deprotonation by a strong base to form a phosphonium ylide. This ylide is a highly reactive species that can then react with a carbonyl compound, such as an aldehyde or ketone, leading to the formation of a carbon-carbon double bond. The Wittig reaction is widely utilized in organic chemistry to prepare alkenes, which are important building blocks in the synthesis of a variety of organic compounds, including pharmaceuticals, agrochemicals, and polymers.

Propyltriphenylphosphonium bromide is also used in other reactions that involve phosphonium ylides, such as in the formation of complex organic molecules. The ability of these ylides to participate in nucleophilic substitutions and additions makes them versatile reagents for the synthesis of a wide range of chemical compounds.

In addition to its role in organic synthesis, propyltriphenylphosphonium bromide has applications in phase transfer catalysis. Phase transfer catalysis is a technique used to facilitate reactions between two substances that are in different phases, typically where one reactant is in an aqueous phase and the other is in an organic phase. Propyltriphenylphosphonium bromide can assist in the transport of ionic species between these phases, thereby improving reaction rates and efficiency. This makes it useful in processes such as alkylation, esterification, and other transformations involving ionic reactants.

The compound is also studied in the context of organophosphorus chemistry, which includes the synthesis of various phosphonium salts and their derivatives. These compounds are valuable for the development of new materials, including phosphonium-based ionic liquids, which are increasingly used in catalysis, electrochemistry, and solvent extraction processes due to their unique properties.

As with other phosphonium salts, propyltriphenylphosphonium bromide should be handled with care. It can be irritating to the skin, eyes, and respiratory system, and appropriate safety measures, including the use of gloves, goggles, and working in a well-ventilated area, should be observed.

In summary, propyltriphenylphosphonium bromide is an important chemical compound used in organic synthesis, particularly in the Wittig reaction and phase transfer catalysis. Its ability to generate reactive ylides and facilitate the transfer of ions between different phases makes it a valuable reagent in the synthesis of alkenes and other organic compounds. Additionally, it plays a significant role in the development of organophosphorus chemistry and the design of new materials for advanced chemical applications.

References

2014 Incorporation of triphenylphosphonium functionality improves the inhibitory properties of phenothiazine derivatives in Mycobacterium tuberculosis Bioorganic & Medicinal Chemistry
DOI: 10.1016/j.bmc.2014.07.050

2024 Synthesis of oxanorbornene-based phosphonium polymeric ionic liquids (PILs) and investigation of their electrical properties Mater. Adv.
DOI: 10.1039/D3MA00630A

2018 Dehydrochlorination of 1,2-dichloroethane over a tetraphenylphosphonium chloride-supported carbon catalyst New J. Chem.
DOI: 10.1039/C8NJ02580K