2-Nitrophenol → HCID 86740816, compound
Reaction equation
[OH-].[Ba+2:2].[OH-].[N+:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[OH:13])([O-:6])=[O:5]>O>[N+:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O-:13])([O-:6])=[O:5].[Ba+2:2].[N+:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O-:13])([O-:6])=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 75 °C
Procedure
Heat 3 1. of distilled water in a 4-1. flask to 75° C. on a steam bath. Add 16.67 g. of barium hydroxide, [Ba(OH)2.8H2O] and 21.67 g. of o-nitrophenol. Stir vigorously for 1 hour at 75° C. and let stand overnight at room temperature. Decant to another flask, heat to 75° C., add 4.17 g. of o-nitrophenol, stir and let stand overnight at room temperature. Decant and filter on a Buchner funnel through Whatman No. 4 paper and adjust the filtrate to 3 1. with distilled water.
Workup
- temperatureHeat 3 1
- customto 75° C.
- additionAdd 16.67 g
- waitlet stand overnight at room temperature
- customDecant to another flask
- temperatureheat to 75° C.
- additionadd 4.17 g
- stirringof o-nitrophenol, stir
- waitlet stand overnight at room temperature
- customDecant
- filtrationfilter on a Buchner funnel through Whatman No
Sources & evidence
- ORD record
- ord-6a97af991d2f43838839c49b027d044f
- Source dataset
- uspto-grants-1986_08
- Patent number
- US04605721
Reaction notes
Loading…