Bromophenols
In chemistry, bromophenols form a group of substances which are formally derived from phenol and bromobenzene . The structure consists of a benzene ring with a hydroxyl group (–OH) and bromine (–Br) as substituents . Their arrangement results in three constitutional isomers with the empirical formula C 6 H 5 BrO.
Bromophenols | ||||||||
Surname | 2-bromophenol | 3-bromophenol | 4-bromophenol | |||||
other names | o -Bromophenol | m -bromophenol | p -bromophenol | |||||
Structural formula | ||||||||
CAS number | 95-56-7 | 591-20-8 | 106-41-2 | |||||
PubChem | 7244 | 11563 | 7808 | |||||
Molecular formula | C 6 H 5 BrO | |||||||
Molar mass | 173.02 g mol −1 | |||||||
Physical state | liquid | firmly | ||||||
Melting point | 3-7 ° C | 28-32 ° C | 61-64 ° C | |||||
boiling point | 195-196 ° C | 236 ° C | 235-236 ° C | |||||
pK s value | 8.42 | 9.11 | 9.34 | |||||
GHS labeling |
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H and P phrases | 226-302-315-319-335-400 | 315-319-335 | 302-315 | |||||
no EUH phrases | no EUH phrases | no EUH phrases | ||||||
261-273-305 + 351 + 338 | 261-305 + 351 + 338 | 301 + 312 + 330 |
properties
4-bromophenol, which has the highest symmetry, has the highest melting point. The bromophenols are more acidic than phenol due to the −I effect of the bromine substituent. The pK s values are therefore correspondingly lower (phenol: 9.99).
presentation
2-Bromophenol can be obtained from phenol via the bromination of the sodium salt of 2,4-disulfonic acid.
The preparation from 2-bromoaniline is also possible.
3-Bromophenol can be produced from nitrobenzene by bromination, diazotization and subsequent boiling of the diazonium salt .
4-Bromophenol is obtained from phenol by bromination with elemental bromine.
Individual evidence
- ↑ a b c data sheet 2-bromophenol from Sigma-Aldrich , accessed on November 3, 2016 ( PDF ).
- ↑ a b c data sheet 3-bromophenol from Sigma-Aldrich , accessed on November 3, 2016 ( PDF ).
- ↑ a b c data sheet 4-bromophenol from Sigma-Aldrich , accessed on November 3, 2016 ( PDF ).
- ↑ a b CRC Handbook of Tables for Organic Compound Identification , Third Edition, 1984, ISBN 0-8493-0303-6 .
- ↑ Ralph C. Huston and Murel M. Ballard: o-Bromophenol In: Organic Syntheses . 14, 1934, p. 14, doi : 10.15227 / orgsyn.014.0014 ; Coll. Vol. 2, 1943, p. 97 ( PDF ).
- ↑ Joachim Buddrus: Fundamentals of organic chemistry ; ISBN 978-3-11-014683-7 .
- ^ Association of authors: Organikum , 19th edition, Johann Ambrosius Barth, Leipzig · Berlin · Heidelberg 1993, ISBN 3-335-00343-8 , pp. 331-332.