3-Hydroxybenzoic Acid → 4-Bromo-3-hydroxybenzoic acid
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].[Br:11]Br>C(O)(=O)C>[Br:11][C:10]1[CH:9]=[CH:8][C:4]([C:5]([OH:7])=[O:6])=[CH:3][C:2]=1[OH:1]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
This acid was prepared in similar way to that described by Buehler et al (Buehler, C. A., Harris, J. O., Shacklett, C and Block, B. P.; J. Am. Chem. Soc., 68, 574-577 (1946)). To a stirred suspension of 3-hydroxybenzoic acid (50.0 g, 0.362 mol) in acetic acid (495 ml), at RT under argon, was added a solution of bromine (57.97 g, 0.3627 mol) in acetic acid (192 ml) over 2 h. During the addition the internal temperature rose from 18.0 to 22.0° C. The mixture was stirred for 21 h and then concentrated under vacuum, where approximately (500 ml) of distillate was collected. The resulting concentrated solution was stored at 4° C. for 2 h. The resulting white solid was filtered off and washed with cold water (100 ml). This solid was dissolved in a minimum volume of boiling water (220 ml), filtered and allowed to cool to room temperature. The resulting solid was removed by filtration, washed with cold water and dried in a vacuum oven at 58° C. to give the title compound (12.50 g, yield 15.9%), mp=231-232° C., (lit mp 225-226° C.)1.
Workup
- customThis acid was prepared in similar way to
- additionDuring the addition the internal temperature
- customrose from 18.0 to 22.0° C
- concentrationconcentrated under vacuum, where approximately (500 ml) of distillate
- customwas collected
- waitThe resulting concentrated solution was stored at 4° C. for 2 h
- filtrationThe resulting white solid was filtered off
- washwashed with cold water (100 ml)
- dissolutionThis solid was dissolved in a minimum volume of boiling water (220 ml)
- filtrationfiltered
- customThe resulting solid was removed by filtration
- washwashed with cold water
- customdried in a vacuum oven at 58° C.
Sources & evidence
- ORD record
- ord-711399c6fc6345198d0513dab30cb773
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06787550B1
Reaction notes
Loading…