5333-62-0

Basic information

• Product Name: (Trityloxymethyl)benzene
• Synonyms: (Trityloxymethyl)benzene;Benzyl trityl ether;Benzyl(triphenylmethyl) ether;Benzyltrityl ether;Tritylbenzyl ether
• CAS NO: 5333-62-0
• Molecular Formula: C₂₆H₂₂O
• Molecular Weight: 350.4523
• Mol File: 5333-62-0.mol
• Article Data: 22

Chemical Properties

• Boiling Point: 463.8°Cat760mmHg
• Flash Point: 260.3°C
• Appearance: /
• Density: 1.107g/cm³
• Vapor Pressure: 2.44E-08mmHg at 25°C
• Refractive Index: 1.614
• CAS DataBase Reference: (Trityloxymethyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (Trityloxymethyl)benzene(5333-62-0)
• EPA Substance Registry System: (Trityloxymethyl)benzene(5333-62-0)

Safety Data

• Hazardous Substances Data: 5333-62-0(Hazardous Substances Data)

Usage

General Description

"(Trityloxymethyl)benzene" is a compound consisting of a benzene ring with a trityloxymethyl group attached to it. The trityloxymethyl group is a protective group commonly used in organic synthesis to block the reactivity of certain functional groups. It is often used to protect alcohols and phenols. (Trityloxymethyl)benzene is used in the synthesis of a variety of organic molecules and can be utilized as a building block in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and reactivity make it a valuable tool in organic chemistry.

InChI:InChI=1/C26H22O/c1-5-13-22(14-6-1)21-27-26(23-15-7-2-8-16-23,24-17-9-3-10-18-24)25-19-11-4-12-20-25/h1-20H,21H2

Upstream product

• 60-29-7 diethyl ether 
• 120-51-4 benzoic acid benzyl ester 
• 16002-63-4 phenylmagnesium iodide 
• 76-84-6 triphenylmethyl alcohol 
• 100-51-6 benzyl alcohol 
• 76-83-5 trityl chloride 
• 132814-50-7 C₂₆H₂₁LiO 
• 78646-25-0 4-dimethylamino-1-N-(triphenylmethyl)pyridinium chloride 
• 87839-57-4 1-(Triphenylmethyl)-4(1H)-pyridon 
• 87839-59-6 N-trityl-2(1H)-pyridone 
• 87839-55-2 2-pyridyl trityl ether 
• 437-17-2 tritylium hexafluorophosphate 
• 267881-66-3 allylbenzyloxy-t-butylmethylsilane 
• 1140622-58-7 2'-deoxy-3',5'-bis-O-triphenylmethyluridine 

Downstream Products

• 519-73-3 triphenylmethane 
• 100-52-7 benzaldehyde 
• 58352-81-1 3-Trityloxy-butyric acid ethyl ester 
• 116021-13-7 (2S)-2-methyl-3-(trityloxy)propionic acid methyl ester 
• 123077-62-3 ethyl (S)-2-(trityloxy)propionate 
• 80595-15-9 (1R)-1-phenyl-2-O-triphenylmethyl-1,2-ethanediol 
• 68883-09-0 1,2-bis-trityloxy-ethane 
• 114102-89-5 o-nitrophenyl 6-O-trityl-β-D-galactopyranoside 
• 10276-85-4 benzyl caprylate 
• 140-11-4 Benzyl acetate 
• 100-51-6 benzyl alcohol 
• 27552-66-5 5′-O-tritylguanosine 
• 6554-10-5 5'-O-trityluridine 
• 18048-85-6 5'-O-(triphenylmethyl)adenosine 

Relevant articles and documents

Temporal control in tritylation reactions through light-driven variation in chloride ion binding catalysis-a proof of concept

Tripodal triazole-linked azo(hetero)arene-based photoswitchable catalysts T1-5 have been designed, synthesized and optimized for the tritylation reaction of benzylamine (BzNH2). The tritylation reaction rates/yields achieved by light induced isomerization are compared between the native and photoswitched states of the catalyst T1. This concept of controlling the tritylation reaction rates with light has also been extended to additional substrates. The critical role of the triazole C-H?Cl- interactions has been confirmed by a combination of spectroscopic, calorimetric and computational studies. Also, the effect of variation in the binding affinities between the native and photoswitched states of the catalyst at room temperature in the temporal control of the catalysis has been demonstrated. This journal is

Stereoselective and Enantiospecific Mono- and Bis-C?H Azidation of Tr?ger Bases: Insight on Bridgehead Iminium Intermediates and Application to Anion-Binding Catalysis

In the context of Tr?ger base chemistry, regio- and stereoselective Csp3?H azidation reactions are reported. Azide functional groups are introduced at either one or the two benzylic positions selectively. Mild conditions and good yields are aff

Gold(I)-catalyzed synthesis of unsymmetrical ethers using alcohols as alkylating reagents

A microwave-irradiated alcohol-protecting strategy based on gold catalysis utilizing benzyl alcohol, tert-butyl alcohol and triphenylmethanol as alkylating reagents has been developed. This protecting strategy has wide functional group tolerance with satisfactory yields for the majority of the selected alcohols. The mechanism of this transformation was probed with oxygen-18 isotope labelled alcohols assisted by GC-MS techniques and chemical kinetic experiments. This strategy provides an efficient, straightforward and alternative approach to the preparation of benzyl, tert-butyl and trityl ethers in organic synthesis.