2,3-Dichlorobenzoic acid → HCID 86589047, compound
Reaction equation
[N+]([C:4]1[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=1[NH2:6])([O-])=O.Cl[C:12]1[C:20]([Cl:21])=[CH:19][CH:18]=[CH:17][C:13]=1[C:14]([OH:16])=[O:15].C(=O)([O-])[O-].[Na+].[Na+]>CS(C)=O>[C:5]1([NH:6][C:20]2([Cl:21])[CH:19]=[CH:18][CH:17]=[C:13]([C:14]([OH:16])=[O:15])[CH2:12]2)[CH:7]=[CH:8][CH:9]=[CH:10][CH:4]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 110 °C
Procedure
To a stirred solution of 20.0 g (0.145 mole) of 2-nitroaniline 1, 28.0 g (0.146 mole) of 2,3-dichlorobenzoic acid in 200 mL dry dimethyl sulfoxide, 20.0 g (0.19 mole) of anhydrous sodium carbonate is added. The reaction mixture is heated at 110° C. for 5 hours under nitrogen atmosphere. The dimethyl sulfoxide solvent from the reaction mixture is removed under high vacuum and dried. The crude product is extracted three times each time with 100 mL methylene chloride by partitioning into water. The combined methylene chloride layer is dried over anhydrous sodium sulfate and filtered. Solvent from the filtrate is removed under reduced pressure and dried. The crude residue is chromatographed on a silica gel 60 column (230-400 mesh) using 25% ethyl acetate in hexane as an elution solvent. The fractions containing the desired product are combined and the solvent removed under reduced pressure to yield 20.0 g (47%) of N-phenyl N-(1-chloro 3-carboxyphenyl) amine 9.
Workup
- customThe dimethyl sulfoxide solvent from the reaction mixture is removed under high vacuum
- customdried
- extractionThe crude product is extracted three times each time with 100 mL methylene chloride
- customby partitioning into water
- dry with materialThe combined methylene chloride layer is dried over anhydrous sodium sulfate
- filtrationfiltered
- customSolvent from the filtrate is removed under reduced pressure
- customdried
- customThe crude residue is chromatographed on a silica gel 60 column (230-400 mesh)
- additionThe fractions containing the desired product
- customthe solvent removed under reduced pressure
Sources & evidence
- ORD record
- ord-22ec86ec3ac24b3b801783e3f64f4ab4
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07674886B2
Reaction notes
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