Bromotoluene Explained

Bromotoluenes are aryl bromides based on toluene in which at least one aromatic hydrogen atom is replaced with a bromine atom. They have the general formula C7H8–nBrn, where n = 1–5 is the number of bromine atoms.

Monobromotoluene

Monobromotoluenes are bromotoluenes containing one bromine atom. There are three isomers, each with the formula C7H7Br.

Properties

The isomers differ in the location of the bromine, but have the same chemical formula.

align="center" colspan="4" Monobromotoluene isomers[1] [2] [3]
Common name
Structure
Systematic name1-bromo-2-methylbenzene1-bromo-3-methylbenzene1-bromo-4-methylbenzene
Molecular formulaC7H7Br (C6H4BrCH3)
Molar mass171.03 g/mol
Appearancecolorless liquidcolorless liquidwhite crystalline solid
CAS number[95-46-5][591-17-3][106-38-7]
align="center" colspan="5" Properties
Density and phase1.431 g/ml, liquid1.4099 g/ml, liquid1.3995 g/ml, solid
Solubility in waterpractically insoluble
Other solubilitiesvery soluble in ethanol, ether, benzene, carbon tetrachloride, acetone, chloroform
Melting point-27.8 °C (-18.0 °F; -409.63 K)-39.8 °C (-39.6 °F; -388.03 K)28.5 °C (83.3 °F; 301.7 K)
Boiling point181.7 °C (359.1 °F; 454.9 K)183.7 °C (362.7 °F; 456.9 K)184.5 °C (364.1 °F; 457.7 K)

Benzyl bromide is an isomer, which has a bromine substituted for one of the hydrogens of toluene's methyl group, and it is sometimes named α-bromotoluene.

Preparation

A laboratory route to p-bromotoluene proceeds from p-toluidine, which is diazotiized followed by treatment with copper(I) bromide.[4]

Uses

Bromotoluenes are precursors to many organic building blocks. For example, the methyl group may be oxidized using potassium permanganate to form the corresponding bromobenzoic acid.[5] The methyl group may also be partially oxidized to form bromobenzaldehyde.[6]

See also

Notes and References

  1. 7236. 2-Bromotoluene. January 19, 2023.
  2. 11560. 3-Bromotoluene. January 19, 2023.
  3. 7805. 4-Bromotoluene. January 19, 2023.
  4. Bigelow . L. A. . 1925 . p-BROMOTOLUENE . . 5 . 21 . 10.15227/orgsyn.005.0021.
  5. Bigelow . L. A. . A Study of Side-Chain Oxidations with Potassium Permanganate. Ii . 1922 . . 44 . 9 . 2010–2019 . 10.1021/ja01430a020.
  6. Coleman . G. H. . Honeywell . G. E. . 1937 . p-BROMOBENZALDEHYDE . . 17 . 20 . 10.15227/orgsyn.017.0020.