84563-54-2

  • Product Name:Bis(4-tert-butylphenyl)iodonium trifluoromethanesulfonate
  • Molecular Formula:C21H26F3IO3S
  • Purity:99%
  • Molecular Weight:542.401
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Product Details

pd_meltingpoint:237 °C(lit.)

Purity:99%

Quality Factory Hot Selling Bis(4-tert-butylphenyl)iodonium trifluoromethanesulfonate 84563-54-2 with Fast Shipping

  • Molecular Formula:C21H26F3IO3S
  • Molecular Weight:542.401
  • Melting Point:237 °C(lit.)
     
  • PSA:65.58000 
  • LogP:3.54220 

BIS(4-TERT-BUTYLPHENYL)IODONIUM TRIFLATE(Cas 84563-54-2) Usage

InChI:InChI=1/C20H26I.CHF3O3S/c1-19(2,3)15-7-11-17(12-8-15)21-18-13-9-16(10-14-18)20(4,5)6;2-1(3,4)8(5,6)7/h7-14H,1-6H3;(H,5,6,7)/q+1;/p-1

84563-54-2 Relevant articles

Transition Metal-Free N-Arylation of Amino Acid Esters with Diaryliodonium Salts

Kervefors, Gabriella,Kersting, Leonard,Olofsson, Berit

supporting information, p. 5790 - 5795 (2021/03/08)

A transition metal-free approach for the...

N1- and N3-Arylations of Hydantoins Employing Diaryliodonium Salts via Copper(I) Catalysis at Room Temperature

Abha Saikia, Raktim,Barman, Dhiraj,Dutta, Anurag,Jyoti Thakur, Ashim

supporting information, p. 400 - 410 (2020/12/17)

Copper(I)-catalyzed N-arylation (both N1...

Direct Copper-Catalyzed C-3 Arylation of Diphenylphosphine Oxide Indoles

Huang, Xiao-Ling,Li, Chong,Wang, Juan,Yang, Shang-Dong

supporting information, (2021/10/25)

We have developed a simple and effective...

Spatial anion control on palladium for mild C-H arylation of arenes

Dhankhar, Jyoti,González-Fernández, Elisa,Dong, Chao-Chen,Mukhopadhyay, Tufan K.,Linden, Anthony,?ori?, Ilija

supporting information, p. 19040 - 19046 (2020/11/13)

C-H arylation of arenes without the use ...

84563-54-2 Process route

tert-butylbenzene
253185-03-4,253185-04-5

tert-butylbenzene

trifluorormethanesulfonic acid
1493-13-6

trifluorormethanesulfonic acid

1-tert-butyl-4-iodobenzene
35779-04-5

1-tert-butyl-4-iodobenzene

bis(4-tert-butylphenyl)iodonium trifluoromethanesulfonate
84563-54-2

bis(4-tert-butylphenyl)iodonium trifluoromethanesulfonate

Conditions
Conditions Yield
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃;
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 1h; Inert atmosphere; Schlenk technique; Sealed tube;
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃;
With m-chloroperoxybenzoic acid; In dichloromethane; at 0 ℃; Sealed tube;
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at -78 ℃; for 3h; Temperature; Solvent; Sealed tube;
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 - 20 ℃; for 3.16667h;
tert-butylbenzene
253185-03-4,253185-04-5

tert-butylbenzene

trifluorormethanesulfonic acid
1493-13-6

trifluorormethanesulfonic acid

bis(4-tert-butylphenyl)iodonium trifluoromethanesulfonate
84563-54-2

bis(4-tert-butylphenyl)iodonium trifluoromethanesulfonate

Conditions
Conditions Yield
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 0.166667h;
78%
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 - 20 ℃; for 0.416667h;
78%
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 0.166667h;
78%
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 0.166667h;
78%
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 0.333333h;
78%
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 0.333333h;
78%
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 0.333333h; Sealed tube;
78%
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 - 20 ℃; for 0.333333h;
78%
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 0.333333h;
78%
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 1h;
78%
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 1h; Inert atmosphere; Sealed tube;
77%
With iodine; 3-chloro-benzenecarboperoxoic acid; In 1,2-dichloro-ethane; at 20 ℃; for 0.0166667h; Inert atmosphere; Flow reactor; Sonication;
70%
tert-butylbenzene; With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 ℃; for 0.5h; Reflux;
trifluorormethanesulfonic acid; In dichloromethane; at 20 ℃; for 6h;
64.5%
tert-butylbenzene; With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 ℃; for 0.0833333h;
trifluorormethanesulfonic acid; at 0 - 20 ℃; for 2.08333h;
57%
tert-butylbenzene; With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 ℃; for 0.166667h;
trifluorormethanesulfonic acid; In dichloromethane; at 0 ℃;
50%
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 - 20 ℃; for 2h;
43%
With iodine; 3-chloro-benzenecarboperoxoic acid;
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; water; at 0 - 20 ℃; for 0.333333h; Schlenk technique; Inert atmosphere;
With iodine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; Inert atmosphere;

84563-54-2 Upstream products

  • 253185-03-4
    253185-03-4

    tert-butylbenzene

  • 1493-13-6
    1493-13-6

    trifluorormethanesulfonic acid

  • 358-23-6
    358-23-6

    trifluoromethylsulfonic anhydride

  • 35779-04-5
    35779-04-5

    1-tert-butyl-4-iodobenzene

84563-54-2 Downstream products

  • 1151782-18-1
    1151782-18-1

    (E)-1-(tert-butyl)-4-(3,3-dimethylbut-1-en-1-yl)benzene

  • 1374007-21-2
    1374007-21-2

    N-(4-(tert-butyl)phenyl)-S,S-dimethylsulfoximine

  • 1374007-20-1
    1374007-20-1

    N-(4-(tert-butyl)phenyl)-S-methyl-S-(4-methylphenyl)-sulfoximine

  • 1392826-96-8
    1392826-96-8

    (E)-3-(4-tert-butylphenyl)-2-propen-1-ol acetate