Production Method 1

78600-33-6

943899-12-5

Reaction Conditions

1.1 Reagents: Butyllithium Solvents: Tetrahydrofuran ;  -78 °C; 1 h, rt; rt → -78 °C
1.2 Reagents: Triethyl borate ;  -78 °C; 12 h, rt
1.3 Reagents: Hydrochloric acid Solvents: Water

Reference

Organic light-emitting diodes using phenylanthracene derivatives with carbazole analog substituents or fluorene derivatives

, European Patent Organization, , ,

Production Method 2

78600-33-6

943899-12-5

Reaction Conditions

1.1 Reagents: Butyllithium ,  Triisopropyl borate Solvents: Hexane ;  0 °C; 1 h, 0 °C
1.2 Reagents: Hydrochloric acid Solvents: Water

Reference

Organic light-emitting diode materials based on donor and acceptor group-containing compounds and light-emitting devices using them

, World Intellectual Property Organization, , ,

Production Method 3

78600-33-6

943899-12-5

Reaction Conditions

1.1 Reagents: Butyllithium Solvents: Tetrahydrofuran ,  Hexane ;  -78 °C; 1 h, -78 °C
1.2 Reagents: Triisopropyl borate ;  -78 °C; -78 °C → rt; 12 h, rt

Reference

Novel organic electroluminescent compounds and organic electroluminescent device using the same

, World Intellectual Property Organization, , ,

Production Method 4

89598-96-9

943899-12-5

Reaction Conditions

1.1 rt → 150 °C; 4 - 48 h, 50 - 150 °C

Reference

1,2,4-Thiadiazole compound, and its preparation method and application as light emitting layer material of OLED (organic light emitting device)

, World Intellectual Property Organization, , ,

Production Method 5

89598-96-9

943899-12-5

Reaction Conditions

1.1 rt → 150 °C; 4 - 48 h, 50 - 150 °C

Reference

1,2,4-Thiadiazole compound, and its preparation method and application as light emitting layer material of OLED

, China, , ,

Production Method 6

943899-12-5

Reaction Conditions

Reference

Preparation of heterocyclic compound for organic electronic device

, World Intellectual Property Organization, , ,

(3-(Diphenylamino)phenyl)boronic acid Raw materials

• 3-Bromotriphenylamine
• 3-Bromophenylboronic acid

(3-(Diphenylamino)phenyl)boronic acid Preparation Products

• (3-(Diphenylamino)phenyl)boronic acid (943899-12-5)

• 1. Estimation of fusel-oil in spirits
  Analyst, 1890,15, 203-209
• 2. Excited-state proton-coupled electron transfer within ion pairs?
  Gerald J. Meyer,Leif Hammarstr?m Chem. Sci., 2020,11, 3460-3473
• 3. Excimer–monomer switch: a reaction-based approach for selective detection of fluoride?
  Qiao Song,Angela Bamesberger,Lingyun Yang,Haley Houtwed,Haishi Cao Analyst, 2014,139, 3588-3592
• 4. Distinctive size effects of Pt nanoparticles immobilized on Fe3O4@PPy used as an efficient recyclable catalyst for benzylic alcohol aerobic oxidation and hydrogenation reduction of nitroaromatics
  Yu Long,Bing Yuan,Jianrui Niu,Xin Tong,Jiantai Ma New J. Chem., 2015,39, 1179-1185
• 5. Elusive 2-aminofuran Diels–Alder substrates for a straightforward synthesis of polysubstituted anilines?
  Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555

• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Amines Tertiary amines

• 178752-79-9((3-(dimethylamino)phenyl)boronic acid)
• 302348-49-8(4-(Methylamino)phenylboronic acid)
• 1256355-23-3(3-Dimethylaminophenylboronic acid, hydrochloride)
• 201802-67-7(4-(Diphenylamino)benzeneboronic acid)
• 28611-39-4((4-(dimethylamino)phenyl)boronic acid)
• 877064-60-3(3-(methylamino)phenylboronic acid)
• 503299-18-1(Boronic acid, [6-(diphenylamino)-2-naphthalenyl]-)
• 1150114-73-0([4-(dimethylamino)phenyl]boronic acid;hydrochloride)
• 717888-41-0((4-(Naphthalen-1-yl(phenyl)-amino)phenyl)boronic acid)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)