T83801
Trityl chloride
97%
Synonym(s):
Chlorotriphenylmethane, Triphenylchloromethane, Triphenylmethyl chloride
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About This Item
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Quality Level
Assay
97%
bp
230-235 °C/20 mmHg (lit.)
mp
109-112 °C (lit.)
SMILES string
ClC(c1ccccc1)(c2ccccc2)c3ccccc3
InChI
1S/C19H15Cl/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
InChI key
JBWKIWSBJXDJDT-UHFFFAOYSA-N
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Application
Protecting reagent for amines, alcohols, and thiols.
Trityl chloride can be used as a catalyst:
- In Ritter type synthesis of 1-amidoalkyl-2-naphtols through a one-pot three-component reaction of naphthol, aryl aldehydes and acetonitrile.
- In the synthesis of 1,2,4,5-tetrasubstituted imidazoles via a one-pot multi-component reaction of benzil with aldehydes, primary amines, and ammonium acetate.
- In the preparation of amido alkyl phenols via one-pot, multi-component reaction of phenols, aromatic aldehydes, and amides under solvent-free conditions.
- In one-pot, multi-component synthesis of substituted piperidines using aromatic aldehydes, amines, and β-ketoesters.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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One pot synthesis of 1, 2, 4, 5-tetrasubstituted-imidazoles catalyzed by trityl chloride in neutral media
Royal Society of Chemistry Advances, 4(105), 60636-60639 (2014)
Tetrahedron Letters, 48, 5017-5017 (2007)
Trityl chloride as an efficient organic catalyst for the synthesis of 1-amidoalkyl-2-naphtols in neutral media at room temperature
Applied Catalysis A: General, 386(1-2), 179-187 (2010)
Protective Groups in Organic Synthesis (1991)
Solvent-free preparation of amidoalkyl phenols catalyzed by trityl chloride under neutral media
Canadian Journal of Chemistry, 93(11), 1245-1248 (2015)
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