32247-96-4

  • Product Name:3,5-Bis(Trifluoromethyl)Benzyl Bromide
  • MF:C9H5BrF6
  • Purity:99%
  • Molecular Weight:307.033
Inquiry

Product Details

Good factory exports good 3,5-Bis(Trifluoromethyl)Benzyl Bromide 32247-96-4

  • Molecular Formula:C9H5BrF6
  • Molecular Weight:307.033
  • Appearance/Colour:colorless to yellow brown Clear liquid 
  • Vapor Pressure:1.34mmHg at 25°C 
  • Melting Point:18°C 
  • Refractive Index:n20/D 1.445(lit.)  
  • Boiling Point:178.3 °C at 760 mmHg 
  • Flash Point:26.1 °C 
  • PSA:0.00000 
  • Density:1.651 g/cm3 
  • LogP:4.61910 

3,5-Bis(trifluoromethyl)benzyl bromide(Cas 32247-96-4) Usage

Synthesis

Synthesis of 3, 5-bis (trifluoromethyl)-benzyl bromide:In a 4-neck flask with capacity 1000 ml equipped with mechanical agitator, thermometer, bubble condenser and 100 ml loading funnel, 262.2 g of the product of Example 1 (ii) at 92. 8% (0. 988 moles), 550,2 g HBr 48% (3.2645 moles) are loaded; this is heated at 50°C so as to melt the alcohol, then one starts to dose 113 g of concentrated His04 (1.153 moles). Pouring is accomplished in 30 minutes, noting an increase of the internal temperature. This is heated to 100-105°C and left to react for 8 hours. The reaction is completed by reflux heating for per 1.5 hours. the mixture is left to settle and the phases are separated; the solvents are removed from the organic phase and the product in the title is obtained with a yield of 99.1 %.

InChI:InChI=1/C9H5BrF6/c10-4-5-1-6(8(11,12)13)3-7(2-5)9(14,15)16/h1-3H,4H2

32247-96-4 Relevant articles

One-Step Synthesis of Substituted Benzofurans from ortho- Alkenylphenols via Palladium-Catalyzed C=H Functionalization

Yang, Dejun,Zhu, Yifei,Yang, Na,Jiang, Qiangqiang,Liu, Renhua

supporting information, p. 1731 - 1735 (2016/06/09)

A dehydrogenative oxygenation of C(sp2)=...

PROCESS FOR THE PREPARATION 3,5-BIS(TRIFLUOROMETHYL)BENZYLALCOHOL

-

Page/Page column 7-8, (2010/02/11)

The present invention concerns a process...

N-acylamino benzyl ether derivatives

-

, (2008/06/13)

This invention relates to N-acylamino ar...

Scavenger assisted combinatorial process for preparing libraries of tertiary amine compounds

-

, (2008/06/13)

This invention relates to a novel soluti...

32247-96-4 Process route

3,5-bis(trifluoromethyl)benzenemethanol
32707-89-4

3,5-bis(trifluoromethyl)benzenemethanol

3,5-bis(trifluoromethyl)benzyl bromide
32247-96-4

3,5-bis(trifluoromethyl)benzyl bromide

Conditions
Conditions Yield
With sulfuric acid; hydrogen bromide; In water; at 50 - 105 ℃; for 10h; Heating / reflux;
99.1%
With phosphorus tribromide; In dichloromethane; for 0.5h; Cooling with ice;
3,5-bis(trifluoromethyl)benzyl bromide
32247-96-4

3,5-bis(trifluoromethyl)benzyl bromide

Conditions
Conditions Yield

32247-96-4 Upstream products

  • 32707-89-4
    32707-89-4

    3,5-bis(trifluoromethyl)benzenemethanol

32247-96-4 Downstream products

  • 132130-91-7
    132130-91-7

    2-(3,5-Bis-trifluoromethyl-benzyloxy)-1,1,2,2-tetrafluoro-ethanesulfonyl fluoride

  • 754-41-6
    754-41-6

    2-(fluorosulfonyl)tetrafluoropropionyl fluoride

  • 132130-92-8
    132130-92-8

    1-(3,5-Bis-trifluoromethyl-benzyloxy)-1,1,2,3,3,3-hexafluoro-propane-2-sulfonyl fluoride

  • 169673-06-7
    169673-06-7

    3,5-bis(trifluoromethyl)benzyl N-(tert-butoxycarbonyl)-L-tryptophanate