Sodium Hydroxide → HCID 59726065, compound
Reaction equation
[NH2:1][C:2]1[C:11]([O:12][CH3:13])=[C:10]([Cl:14])[CH:9]=[C:8]([Cl:15])[C:3]=1[C:4]([O:6]C)=[O:5].[OH-].[Na+]>CO.O>[NH2:1][C:2]1[C:11]([O:12][CH3:13])=[C:10]([Cl:14])[CH:9]=[C:8]([Cl:15])[C:3]=1[C:4]([OH:6])=[O:5]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a stirred solution of aniline 2-3 (11.5 g, 460 mmol) in methanol (250 mL) and H2O (70 mL) was added 2N NaOH (25 mL). The reaction mixture was heated under reflux for 1 h, more 2N NaOH (25 mL) was added and the mixture was heated under reflux for a further 1 h. The solution was cooled and methanol was removed in vacuo. The mixture was dissolved in H2O and extracted with ethyl acetate. The aqueous layer was acidified to pH 2 with conc. HCl. and then extracted into ethyl acetate (×3). The combined extracts were washed with brine, dried over Na2SO4, filtered and concentrated to provide the acid 2-4 as a beige solid (10.4 g, 95% yield). 1H NMR (MeOD, 400 MHz) δ 3.80 (s, 3H), 6.70 (s, 1H).
Workup
- temperatureThe reaction mixture was heated
- temperatureunder reflux for 1 h
- temperaturethe mixture was heated
- temperatureunder reflux for a further 1 h
- temperatureThe solution was cooled
- custommethanol was removed in vacuo
- dissolutionThe mixture was dissolved in H2O
- extractionextracted with ethyl acetate
- extractionand then extracted into ethyl acetate (×3)
- washThe combined extracts were washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-c1ba4336380241c99046296496286f04
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09145375B2
Reaction notes
Loading…