p-Toluenesulfonic acid → HCID 23288677, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[C:9]=1O)[CH:5]=O.[ClH:14].[NH2:15]O.CC1C=CC(S(O)(=O)=O)=CC=1.S([O-])([O-])(=O)=O.[Mg+2]>C1(C)C=CC=CC=1>[Cl:14][C:9]1[C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:4]([C:5]#[N:15])=[CH:3][C:2]=1[OH:1]Participants
Procedure
A mixture of 3,4-dihydroxy-5-nitrobenzaldehyde (5 g, 27.3 mmol), hydroxylamine hydrochloride (2.467 g, 35.5 mmol), tosic acid (0.779 g, 4.10 mmol) and magnesium sulfate (26.3 g, 218 mmol) in toluene (25 ml) was heated at reflux for 6 hours. The reaction mixture was cooled to room temperature, the reaction mixture was partitioned between ethyl acetate and water. The layers were separated and aqueous layer was extracted with ethyl acetate two more times. The combined organic layers were washed with water and brine, dried over magnesium sulfate, filtered and concentrated in vacuo to a small volume and a brown precipitate formed. the precipitate was collected by filtration and after drying under vacuum to give 4.1 g of 4-chloro-3-hydroxy-5-nitrobenzonitrile.
Workup
- temperaturewas heated
- temperatureat reflux for 6 hours
- customthe reaction mixture was partitioned between ethyl acetate and water
- customThe layers were separated
- extractionaqueous layer was extracted with ethyl acetate two more times
- washThe combined organic layers were washed with water and brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo to a small volume
- customa brown precipitate formed
- filtrationthe precipitate was collected by filtration
- customafter drying under vacuum
Sources & evidence
- ORD record
- ord-7c37bc9dc32749778e0d622be801c9c2
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08940736B2
Reaction notes
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