Production Method 1

76-83-5

119-61-9

76-84-6

968-39-8

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 2

3060-50-2

333-60-8

119-61-9

84277-81-6

Reaction Conditions

1.1 Catalysts: 5-[[(2S)-2-[Bis([1,1′:3′,1′′-terphenyl]-5′-yl)[(triethylsilyl)oxy]methyl]-1-pyrr… Solvents: Tetrahydrofuran ,  Water ;  3 d, rt

Reference

Chiral Pyridoxal-Catalyzed Asymmetric Biomimetic Transamination of α-Keto Acids

Shi, Limin; Tao, Chuangan; Yang, Qin; Liu, Yong Ethan; Chen, Jing; et al, Organic Letters, 2015, 17(23), 5784-5787

Production Method 3

93022-10-7

119-61-9

956-89-8

101109-90-4

86-73-7

Reaction Conditions

1.1 Solvents: Benzene ;  600 °C

Reference

Thermal rearrangement of phenyl-substituted ketene ethylene acetals

Oda, Mitsunori; Morimoto, Kazuo; Thanh, Nguyen Chung; Ohta, Reina; Kuroda, Shigeyasu, Heterocycles, 2003, 60(7), 1673-1680

Production Method 4

2983125-18-2

119-61-9

2103741-86-0

Reaction Conditions

1.1 Reagents: Hydrochloric acid Solvents: Tetrahydrofuran ,  Water ;  rt
1.2 Reagents: Sodium bicarbonate Solvents: Water ;  rt

Reference

Unlocking New Prenylation Modes: Azaindoles as a New Substrate Class for Indole Prenyltransferases

Gardner, Eric D.; Johnson, Bryce P.; Dimas, Dustin A.; McClurg, Heather E.; Severance, Zachary C.; et al, ChemCatChem, 2023, 15(19),

Production Method 5

119-61-9

85068-36-6

Reaction Conditions

1.1 Reagents: Bromobenzene ,  Cesium carbonate Catalysts: Triphenylphosphine ,  Palladium diacetate Solvents: o-Xylene ;  16 h, 150 °C; 150 °C → rt
1.2 Reagents: Hydrochloric acid Solvents: Water

Reference

Steric and Electronic Effects Influencing β-Aryl Elimination in the Pd-catalyzed Carbon-Carbon Single Bond Activation of Triarylmethanols

Bour, James R.; Green, Jacob C.; Winton, Valerie J.; Johnson, Jeffrey B., Journal of Organic Chemistry, 2013, 78(4), 1665-1669

Production Method 6

3060-50-2

333-60-8

119-61-9

84277-81-6

Reaction Conditions

1.1 Reagents: Acetic acid Catalysts: 3-Pyridinol, 4-(aminomethyl)-6-methyl-5-[2-[(methylamino)methyl]-1-naphthalenyl]… Solvents: Methanol ,  Water ;  20 h, rt

Reference

Enzyme-inspired axially chiral pyridoxamines armed with a cooperative lateral amine chain for enantioselective biomimetic transamination

Liu, Yong Ethan; Lu, Zhaole; Li, Bo; Tian, Jiaxin; Liu, Feng; et al, Journal of the American Chemical Society, 2016, 138(34), 10730-10733

Production Method 7

3060-50-2

333-60-8

119-61-9

84277-81-6

Reaction Conditions

1.1 Reagents: Acetic acid Catalysts: 2193094-49-2 Solvents: Ethanol ,  Water ;  24 h, 25 °C

Reference

Enantioselective biomimetic transamination of α-keto acids catalyzed by H4-naphthalene-derived axially chiral biaryl pyridoxamines

Hou, Chengkang; Zhao, Guoqing; Xu, Dongfang; Zhao, Baoguo, Tetrahedron Letters, 2018, 59(11), 1028-1033

Benzophenone Raw materials

• (chlorodiphenylmethyl)benzene
• 1H-Pyrrolo[2,3-c]pyridine-3-propanoic acid, α-[(diphenylmethylene)amino]-, ethyl ester
• 2,2-Diphenylglycine
•  
• 1,3-Dioxolane, 2-(diphenylmethylene)-

Benzophenone Preparation Products

• Benzophenone (119-61-9)
• Triphenyl methanol (76-84-6)
• 2,5-Difluorobenzophenone (85068-36-6)
• α,α-Diphenyl-γ-butyrolactone (956-89-8)
• Benzeneacetic acid, α-phenyl-, ethenyl ester (101109-90-4)
• H-Octyl-Gly-OH (84277-81-6)
• Fluorene (86-73-7)
• (Ethoxydiphenylmethyl)benzene (968-39-8)
• ethyl 2-amino-3-{1H-pyrrolo2,3-cpyridin-3-yl}propanoate (2103741-86-0)

• 1. Benzophenone: a ubiquitous scaffold in medicinal chemistry
  Khemchand Surana,Bharatkumar Chaudhary,Monika Diwaker,Satyasheel Sharma Med. Chem. Commun. 2018 9 1803
• 2. Achieving tunable dual-emissive and high-contrast mechanochromic materials by manipulating steric hindrance effects
  Zongliang Xie,Tongtong Su,Eethamukkala Ubba,Huangjun Deng,Zhu Mao,Tao Yu,Ting Zheng,Yi Zhang,Siwei Liu,Zhenguo Chi J. Mater. Chem. C 2019 7 3300
• 3. Mechanistic insights into B–H bond activation with the high-valent oxo-molybdenum complex MoO2Cl2
  Liangfang Huang,Haiyan Wei New J. Chem. 2014 38 5421
• 4. Molecular polarisability. The conformations of diphenyl ketone, dimesityl ketone, and mesityl phenyl ketone as solutes
  P. H. Gore,J. A. Hoskins,R. J. W. Le Fèvre,L. Radom,G. L. D. Ritchie J. Chem. Soc. B 1967 741
• 5. Gas phase dynamics of triplet formation in benzophenone
  Gloria Spighi,Marc-André Gaveau,Jean-Michel Mestdagh,Lionel Poisson,Beno?t Soep Phys. Chem. Chem. Phys. 2014 16 9610

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzophenones
• Natural Products and Extracts Flavors and Fragrances Essential Oils
• Pesticide Chemicals Pesticide Active Ingredients Standard Substances
• Solvents and Organic Chemicals Organic Compounds Aldehyde/Ketone
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons
• Material Chemicals High Polymer Materials
• Natural Products and Extracts Flavors and Fragrances
• Pharmaceutical and Biochemical Products Pharmaceutical Active Ingredients
• Catalysts and Inorganic Chemicals Catalysts

• 825633-33-8(Ethanone, 1,1',1''-[1,3,5-benzenetriyltris(carbonyl-4,1-phenylene)]tris-)
• 2694-78-2(Benzophenone-2,3,4,5,6-d5)
• 2852-68-8(bis(3-methylphenyl)methanone)
• 20912-50-9(4-Benzoylbenzaldehyde)
• 22583-75-1(Benzophenone-d10)
• 109339-64-2(4-Methylbenzophenone-d3)
• 66067-43-4(3-ethylbenzophenone)
• 92756-55-3(Diphenylmethanone;toluene)
• 919356-02-8(Methanone, (4-methylphenyl)[4-[(4-methylphenyl)methyl]phenyl]-)
• 32488-48-5(Benzophenone-13C)