Production Method 1

6310-21-0

881057-14-3

Reaction Conditions

1.1 Reagents: Sodium bicarbonate ,  Iodine Solvents: Water ;  6 h, 0 °C → rt

Reference

Living Polymerization of Bulky Aryl Isocyanide with Arylrhodium Complexes

Onitsuka, Kiyotaka; Yamamoto, Mari; Mori, Tomoko; Takei, Fumie; Takahashi, Shigetoshi, Organometallics, 2006, 25(5), 1270-1278

Production Method 2

6310-21-0

881057-14-3

Reaction Conditions

1.1 Reagents: Sodium bicarbonate ,  Iodine Solvents: Water ;  0 °C; 0 °C → rt; 6 h, rt

Reference

Highly Atroposelective Synthesis of Arylpyrroles by Catalytic Asymmetric Paal-Knorr Reaction

Zhang, Lei; Zhang, Jian; Ma, Ji; Cheng, Dao-Juan; Tan, Bin, Journal of the American Chemical Society, 2017, 139(5), 1714-1717

Production Method 3

6310-21-0

881057-14-3

Reaction Conditions

1.1 Reagents: Sodium bicarbonate ,  Iodine Solvents: Water ;  rt

Reference

Synthesis and characterization of polyimides from 4,4'-(3-(tert-butyl)-4-aminophenoxy)diphenyl ether

Li, Congyan; Yi, Lang; Xu, Shuting; Wu, Xiuming; Huang, Wei; et al, Journal of Polymer Research, 2016, 24(1), 1-9

Production Method 4

6310-21-0

881057-14-3

Reaction Conditions

1.1 Reagents: Sodium bicarbonate ,  Iodine Solvents: Water ;  5 min, 0 °C; 12 h, rt

Reference

Synthesis and characterization of soluble polyimides containing tert-butyl, ether linkages and bisphenol A units

Li, Cong-yan; Yi, Lang; Xu, Shu-ting; Huang, Wei; Yan, De-yue, Gaofenzi Xuebao, 2016, (7), 938-945

Production Method 5

6310-21-0

881057-14-3

Reaction Conditions

1.1 Reagents: Sodium bicarbonate ,  Iodine ;  cooled; 6 h, rt

Reference

A process for preparing 3,3'-di-tert-butylbenzidine

, China, , ,

Production Method 6

6310-21-0

881057-14-3

Reaction Conditions

1.1 Reagents: Sodium bicarbonate ,  Iodine Solvents: Water ;  rt → 0 °C; 0 °C; 0 °C → rt; 6 h, rt

Reference

Enantioselective Synthesis of Axially Chiral N-Aryl-3-methyleneisoindolin-1-ones

Liu, Min; Huang, Min; Li, Wenzhe; Yan, Yingkun; Li, Min; et al, Asian Journal of Organic Chemistry, 2022, 11(8),

Production Method 7

6310-21-0

881057-14-3

Reaction Conditions

1.1 Reagents: Sodium bicarbonate ,  Iodine Solvents: Water ;  0 °C → rt; 12 h, rt

Reference

Soluble aromatic polyimides with high glass transition temperature from benzidine containing tert-butyl groups

Yi, Lang; Li, Congyan; Huang, Wei; Yan, Deyue, Journal of Polymer Research, 2014, 21(11), 1-10

Production Method 8

6310-21-0

881057-14-3

Reaction Conditions

1.1 Reagents: Sodium bicarbonate ,  Iodine Solvents: Water ;  0 °C; 4 h, 0 °C

Reference

N-Heterocyclic Carbene Control over Multiple Stereogenicities: Atroposelective Synthesis of Axially Chiral Phthalimides

Barday, Manuel; Rodrigues, Jessica; Bouillac, Pierre; Rodriguez, Jean; Amatore, Muriel; et al, Advanced Synthesis & Catalysis, 2023, 365(2), 148-155

2-tert-Butyl-4-iodo-phenylamine Raw materials

• 2-tert-butylaniline

2-tert-Butyl-4-iodo-phenylamine Preparation Products

• 2-tert-Butyl-4-iodo-phenylamine (881057-14-3)

• 1. Embedding cyclic nitrone in mesoporous silica particles for EPR spin trapping of superoxide and other radicals?
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• 2. Dissociative electron attachment to HGaF4 Lewis–Br?nsted superacid
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• 3. Excimer formation effects and trap-assisted charge recombination loss channels in organic solar cells of perylene diimide dimer acceptors?
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• 4. Embedding heteroatoms: an effective approach to create porphyrin-based functional materials
  Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
• 5. Exclusive self-aligned β-phase PVDF films with abnormal piezoelectric coefficient prepared via phase inversion?
  N. Soin,D. Boyer,K. Prashanthi,S. Sharma,A. A. Narasimulu,J. Luo,T. H. Shah,E. Siores,T. Thundat Chem. Commun., 2015,51, 8257-8260

• 128318-63-8(4-tert-Butyl-2-iodoaniline)
• 13194-68-8(4-Iodo-2-methylaniline)
• 126832-68-6(Benzenamine, 2,6-diethyl-4-iodo-)
• 76842-13-2(BENZENAMINE, 4-IODO-2-(1-METHYLETHYL)-)
• 193484-13-8(Benzenamine, 5-(1,1-dimethylethyl)-3-iodo-2-methyl-)
• 477738-27-5(Benzenamine, 2-(1,3-dimethylbutyl)-4-iodo-)
• 140411-20-7(Benzenamine, 4-iodo-2,6-bis(1-methylethyl)-)
• 194809-02-4
• 4102-53-8(4-Iodo-2,6-dimethylaniline)
• 99471-67-7((2-Ethyl-4-iodophenyl)amine Hydrochloride)