p-Toluenesulfonic acid → HCID 23288677、化合物
反応式
[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]参加物
実験手順
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.
後処理
- 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
出典と根拠
- ORDレコード
- ord-7c37bc9dc32749778e0d622be801c9c2
- 出典データセット
- uspto-grants-2015_01
- 特許番号
- US08940736B2
反応ノート
読み込み中…