Production Method 1

76-83-5

968-39-8

Reaction Conditions

1.1 Reagents: Sodium bicarbonate ;  12 h, 50 °C

Reference

A Self-Assembled Cage with Endohedral Acid Groups both Catalyzes Substitution Reactions and Controls Their Molecularity

Bogie, Paul M.; Holloway, Lauren R.; Ngai, Courtney; Miller, Tabitha F.; Grewal, Divine K.; et al, Chemistry - A European Journal, 2019, 25(43), 10232-10238

Production Method 2

596-31-6

968-39-8

Reaction Conditions

1.1 Catalysts: Ceric ammonium nitrate Solvents: Ethanol

Reference

Catalytic and efficient cleavage of allylic and tertiary benzylic ethers and esters with Ce(IV)

Iranpoor, Nasser; Mottaghinejad, Enayatolah, Tetrahedron, 1994, 50(24), 7299-306

Production Method 3

132277-76-0

968-39-8

Reaction Conditions

Reference

Single-electron-transfer-initiated thermal reactions of arylmethyl halides. Part 15. The reaction of triphenylmethyl bromide with potassium O-ethyl dithiocarbonate (Potassium xanthate) in benzene and cumene. A note of caution on the application of the radical trap dicyclohexylphosphine as a probe for electron-transfer-initiated reactions of triphenylmethyl halides

Huszthy, Peter; Izso Gergacz, Gyongyi; Lempert, Karoly; Gyor, Miklos; Rockenbauer, Antal, Journal of the Chemical Society, 1990, (1990), 2009-15

Production Method 4

538-51-2

1600-49-3

968-39-8

4553-59-7

1918941-25-9

Reaction Conditions

1.1 Catalysts: p-Toluenesulfonic acid Solvents: Ethanol ,  Dichloromethane ;  1 h, rt

Reference

Trityl Isocyanide as a Mechanistic Probe in Multicomponent Chemistry: Walking the Line between Ugi- and Strecker-type Reactions

Cioc, Razvan C.; Preschel, Hans D.; van der Heijden, Gydo; Ruijter, Eelco ; Orru, Romano V. A., Chemistry - A European Journal, 2016, 22(23), 7837-7842

Production Method 5

87839-57-4

968-39-8

Reaction Conditions

1.1 Solvents: 1,2-Dichloroethane

Reference

Regioselective N- or O-tritylation of 2(1H)-pyridone - (triphenylmethyl)pyridones as tritylation agents

Effenberger, Franz; Brodt, Werner; Zinczuk, Juan, Chemische Berichte, 1983, 116(9), 3011-26

Production Method 6

50653-07-1

968-39-8

Reaction Conditions

1.1 Catalysts: Trimethylsilyl triflate

Reference

Trimethysilyl triflate in organic synthesis. Part 11

Noyori, R.; Murata, S.; Suzuki, M., Tetrahedron, 1981, 37(23), 3899-910

Production Method 7

968-39-8

Reaction Conditions

Reference

Novel synthesis of some mixed arylmethylalkyl ethers

Rutherford, Kenneth G.; Mamer, O. A.; Prokipcak, Joseph M.; Jobin, R. A., Canadian Journal of Chemistry, 1966, 44(19), 2337-9

Production Method 8

76-83-5

968-39-8

119-61-9

76-84-6

Reaction Conditions

1.1 Reagents: Oxygen Solvents: tert-Butylbenzene
1.2 Reagents: Sodium ethoxide

Reference

Single electron transfer initiated thermal reactions of arylmethyl halides. Part 14. The reaction of triphenylmethyl halides with tributylphosphine and tributylamine in apolar solvents

Huszthy, Peter; Izso Gergacz, Gyongyi; Lempert, Karoly; Kajtar-Peredy, Maria; Gyor, Miklos; et al, Journal of the Chemical Society, 1989, (1989), 1513-20

Production Method 9

76-83-5

968-39-8

Reaction Conditions

Reference

The rates of alcoholysis of triarylmethyl chlorides

Nixon, A. C.; Branch, G. E. K., Journal of the American Chemical Society, 1936, 58, 492-8

Production Method 10

76-83-5

968-39-8

Reaction Conditions

1.1 7 h, 150 °C

Reference

New Reaction of Organic Monohalides with Orthoformates

Gazizov, M. B.; Ibragimov, Sh. N.; Khamidullina, O. D.; Karimova, R. F.; Pudovik, M. A.; et al, Russian Journal of General Chemistry, 2005, 75(8), 1325-1326

Production Method 11

76-84-6

968-39-8

Reaction Conditions

1.1 Catalysts: p-Toluenesulfonic acid Solvents: Ethanol ;  rt; rt → 78 °C; 30 min, 78 °C

Reference

Microwave assisted transformation of compounds capable of internal reorientation

Bednarz, Szczepan; Bogdal, Dariusz, Proceedings of the International Electronic Conference on Synthetic Organic Chemistry, 2007, (2007),

Production Method 12

87268-78-8

968-39-8

Reaction Conditions

1.1 Solvents: Ethanol ;  4 h, reflux
1.2 Reagents: Sodium hydroxide Solvents: Water

Reference

Tetrazoles: XLIV. Synthesis and chemical properties of 5-substituted 2-triphenylmethyltetrazoles

Myznikov, L. V.; Artamonova, T. V.; Bel'skii, V. K.; Stash, A. I.; Skvortsov, N. K.; et al, Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii), 2002, 38(9), 1360-1369

Production Method 13

76-83-5

968-39-8

Reaction Conditions

1.1 Reagents: Triethylamine Solvents: Ethanol
1.2 Solvents: Methanol

Reference

Reductive demercuration in deprotection of trityl thioethers, trityl amines, and trityl ethers

Maltese, M., Journal of Organic Chemistry, 2001, 66(23), 7615-7625

Production Method 14

76-83-5

968-39-8

Reaction Conditions

1.1 Reagents: 1,8-Diazabicyclo[5.4.0]undec-7-ene Solvents: Dichloromethane ;  24 h, rt

Reference

Iodine-catalyzed disproportionation of aryl-substituted ethers under solvent-free reaction conditions

Jereb, Marjan; Vrazic, Dejan, Organic & Biomolecular Chemistry, 2013, 11(12), 1978-1999

Production Method 15

76-84-6

968-39-8

Reaction Conditions

Reference

Synthesis of dialkyl ethers by substitution

Tsukamoto, M.; Kitamura, M., Science of Synthesis, 2008, 37, 47-97

Production Method 16

50653-07-1

968-39-8

Reaction Conditions

1.1 Catalysts: Trimethylsilyl triflate

Reference

Trialkylsilyl triflates in organic synthesis. Part 10. A facile procedure for O-tritylation

Murata, S.; Noyori, R., Tetrahedron Letters, 1981, 22(22), 2107-8

Production Method 17

968-39-8

Reaction Conditions

Reference

Triaryl methane derivatives as antiproliferative agents

Al-Qawasmeh, Raed A.; Lee, Yoon; Cao, Ming-Yu; Gu, Xiaoping; Vassilakos, Aikaterini; et al, Bioorganic & Medicinal Chemistry Letters, 2004, 14(2), 347-350

Production Method 18

968-39-8

Reaction Conditions

Reference

Esters of tertiary alcohols

, Japan, , ,

Production Method 19

968-39-8

Reaction Conditions

Reference

A rapid, simple, and mild procedure for alkylation of phenols, alcohols, amides, and acids

Johnstone, Robert A. W.; Rose, Malcolm E., Tetrahedron, 1979, 35(18), 2169-73

Production Method 20

968-39-8

Reaction Conditions

Reference

Interaction of tetraalkoxysilanes with stable carbonium ions

Kursanov, D. N.; Parnes, Z. N.; Kolomnikova, G. D.; Tyulyaev, I. I., Izvestiya Akademii Nauk SSSR, 1972, (1972), 678-80

(Ethoxydiphenylmethyl)benzene Raw materials

• (chlorodiphenylmethyl)benzene
• Triphenyl methanol
• Silane, trimethyl(triphenylmethoxy)-
• 5-Phenyl-2-trityltetrazole
• N,1-diphenylmethanimine
• Carbonodithioic acid, O-ethyl S-(triphenylmethyl) ester
• Benzene,1,1',1''-(isocyanomethylidyne)tris-
• Methyl Triphenylmethyl Ether
• 4(1H)-Pyridinone, 1-(triphenylmethyl)-

(Ethoxydiphenylmethyl)benzene Preparation Products

• Benzophenone (119-61-9)
• Triphenyl methanol (76-84-6)
• 2-phenyl-2-(phenylamino)acetonitrile (4553-59-7)
• (Ethoxydiphenylmethyl)benzene (968-39-8)
• α-(Phenylamino)-N-(triphenylmethyl)benzeneacetamide (1918941-25-9)

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• 574-42-5((Bis(diphenylmethyl)ether))
• 596-31-6(Methyl Triphenylmethyl Ether)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)