Triphenylmethyl chloride
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| Template:Longitem | C19H15Cl |
| Molar mass | 278.7754 g/mol |
| Appearance | white to yellow solid |
| Density | 1.141 g/cm3 |
| Melting point | Template:Chembox CalcTemperatures |
| Boiling point | Template:Chembox CalcTemperatures |
| Solubility | soluble in chloroform, benzene, acetone,[1] ether, THF, hexane[2] |
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Triphenylmethyl chloride or trityl chloride (TrCl) is a white solid with the chemical formula C19H15Cl. It is an alkyl halide, sometimes used to introduce the trityl protecting group.
Preparation
Triphenylmethyl chloride is commercially available. It may be prepared by the reaction of triphenylmethanol with acetyl chloride, or by the Friedel–Crafts alkylation of benzene with carbon tetrachloride to give the trityl chloride-aluminium chloride adduct, which is then hydrolyzed.[3]
Reactions
Triphenylmethylsodium can be prepared from trityl chloride dissolved in an aprotic solvent and sodium:[4]
- (C6H5)3CCl + 2 Na → (C6H5)3CNa + NaCl
Reaction with silver hexafluorophosphate gives triphenylmethyl hexafluorophosphate.
Trityl chloride reacts with zinc in nonpolar solvents (e.g. benzene) to form Gomberg's dimer.[5]
- 2 (C6H5)3CCl + Zn → ((C6H5)3C)2 + ZnCl2
See also
- Triphenylmethyl radical
- Triphenylmethane
- Triphenylmethyl hexafluorophosphate
- Triphenylmethanol
- Gomberg's dimer
References
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