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Iodobenzene diacetate

  • Product Name: Iodobenzene diacetate
  • CAS: 3240-34-4
  • Purity:
  • Appearance: white to light yellow crystal powder

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Factory Supply industrial standard Iodobenzene diacetate 3240-34-4 In Stock

  • Molecular Formula:C10H11IO4
  • Molecular Weight:322.099
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:3.87E-09mmHg at 25°C 
  • Melting Point:161-163 °C(lit.) 
  • Refractive Index:n/D 1.444 
  • Boiling Point:456.8ºC at 760 mmHg 
  • Flash Point:230.1ºC 
  • PSA:52.60000 
  • Density:1.6865 (estimate) 
  • LogP:2.31880 

(Diacetoxyiodo)benzene(Cas 3240-34-4) Usage

Purification Methods

The purity of diacetoxyiodobenzene can be checked by treatment with H2SO4 then KI and the liberated I2 is estimated with standard thiosulfate. It has been recrystallised from 5M acetic acid and dried overnight in a vacuum desiccator over CaCl2. The surface of the crystals may become slightly yellow but this does not affect its usefulness. [Sharefkin & Saltzman Org Synth Coll Vol V 600 1973, Beilstein 5 IV 693.]

General Description

(Diacetoxyiodo)benzene, also known as iodobenzene diacetate (IBD or PIA), is a versatile hypervalent iodine(III) reagent widely used in organic synthesis for oxidative transformations. It serves as an efficient oxidant and mediator in various reactions, including cycloisomerization-amination sequences, oxidative dearomatization, halogenation of indoles, and oxidative alkyl shifts. It is particularly valued for its ability to facilitate metal-free reactions under mild conditions, enabling the synthesis of complex heterocycles, functionalized scaffolds, and bioactive molecules. Additionally, it acts as a key reagent in oxidative cyclizations, intramolecular diaminations, and the preparation of α-acetoxy ketones. Its applications span diverse synthetic strategies, including the construction of natural product skeletons and antimicrobial agents, highlighting its broad utility in modern organic chemistry.

InChI:InChI=1/C6H5I.2C2H4O2/c7-6-4-2-1-3-5-6;2*1-2(3)4/h1-5H;2*1H3,(H,3,4)

3240-34-4 Relevant articles

Applications of hypervalent iodine(III) reagents in constructing ortho-iodo aromatic ethers

Bao-Hua, Hou,De-Jun, Zhou,Ke-Yang, Wang,Peng-Wei, Liu,Xiao-Rui, Cui,Xue-Yan, Li,Xue-Yun, Gong,Yan-Feng, Sun,Yang-Yang, Zhai,Zhen-Hui, Wang

, p. 818 - 822 (2021/04/22)

A one-pot method for the synthesis of ar...

Synthesis of Diverse Aryliodine(III) Reagents by Anodic Oxidation?

Zu, Bing,Ke, Jie,Guo, Yonghong,He, Chuan

supporting information, p. 627 - 632 (2021/02/12)

An anodic oxidation enabled synthesis of...

Preparation and Synthetic Applicability of Imidazole-Containing Cyclic Iodonium Salts

Antonkin, Nikita S.,Vlasenko, Yulia A.,Yoshimura, Akira,Smirnov, Vladimir I.,Borodina, Tatyana N.,Zhdankin, Viktor V.,Yusubov, Mekhman S.,Shafir, Alexandr,Postnikov, Pavel S.

, p. 7163 - 7178 (2021/05/29)

A novel approach to the preparation of i...

Method for producing hypervalent iodine compound

-

Paragraph 0047-0060, (2020/12/31)

The invention provides a method for prod...

3240-34-4 Process route

4-acetoxy-4-tert-butyl-2,5-cyclohexadienone

4-acetoxy-4-tert-butyl-2,5-cyclohexadienone

[bis(acetoxy)iodo]benzene
3240-34-4

[bis(acetoxy)iodo]benzene

hydroquinone monoacetate
3233-32-7

hydroquinone monoacetate

hydroquinone
123-31-9,8027-02-9

hydroquinone

p-benzoquinone
106-51-4

p-benzoquinone

Conditions
Conditions Yield
With perchloric acid; In water; acetonitrile; at 30 ℃; pH=1.0; Further Variations:; pH-values; Reagents; Temperatures; Kinetics;
iodobenzene
591-50-4

iodobenzene

acetic anhydride
108-24-7

acetic anhydride

[bis(acetoxy)iodo]benzene
3240-34-4

[bis(acetoxy)iodo]benzene

Conditions
Conditions Yield
With sodium perborate hexahydrate; acetic acid; at 55 ℃; Inert atmosphere;
91%
acetic anhydride; With dihydrogen peroxide; In water; at 40 ℃; for 4h;
iodobenzene; at 20 - 40 ℃;
83%
With sodium percarbonate; acetic acid; In dichloromethane; at 25 - 40 ℃; for 6.5h;
79%
With sodium periodate; sodium acetate; In acetic acid; for 2h; Heating;
73%
acetic anhydride; With dihydrogen peroxide; In water; at 40 ℃; for 4h;
iodobenzene; In water; at 40 ℃;
71%
With sodium hypochlorite pentahydrate; In acetonitrile; at 20 ℃; for 0.166667h;
70%
With dihydrogen peroxide; at 40 ℃; for 4h;
62%
With urea-hydrogen peroxide; sodium acetate; acetic acid; at 40 ℃; for 3.5h;
44%
With dihydrogen peroxide;
With dihydrogen peroxide;
With dihydrogen peroxide; at 40 ℃; for 4h;
acetic anhydride; With dihydrogen peroxide; at 40 ℃; for 4h;
iodobenzene; Further stages.;
23 g
With sodium periodate; sodium acetate; acetic acid; for 2h; Reflux;

3240-34-4 Upstream products

  • 79-21-0
    79-21-0

    peracetic acid

  • 591-50-4
    591-50-4

    iodobenzene

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    trimethylsilyl acetate

  • 536-80-1
    536-80-1

    iodosylbenzene

3240-34-4 Downstream products

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    2,6-dichloro-1,4-benzoquinone

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    66166-42-5

    2-iodo-4-nitro-1-phenoxybenzene

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    99971-04-7

    4-Nitro-3-(4-nitro-phenoxy)-phenol

  • 66166-39-0
    66166-39-0

    (2-hydroxy-5-nitro-phenyl)-phenyl-iodonium ; acetate

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