反応式
S(Cl)(Cl)=O.[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][C:7]=1[S:15]([OH:18])(=O)=[O:16].S(Cl)(Cl)(=O)=O.[NH4+:24].[OH-]>C1(C)C=CC=CC=1.O1CCCC1.CN(C)C=O>[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][C:7]=1[S:15]([NH2:24])(=[O:18])=[O:16]参加物
8
実験手順
To a solution of thionyl chloride (240 mL) and 2-chloro-5-nitro-benzenesulfonic acid (104 g, 437.6 mmol) was added N,N-dimethylformamide (2 mL) and the reaction mixture was heated up to reflux for 4 hours. The reaction mixture was then carefully quenched into water and the product was isolated by filtration. The sulfonyl chloride 2 was then dissolved in toluene and added to a mixture of NH4OH (520 mL) and tetrahydrofuran (520 mL) at −10° C. After mixing for 1 h, the reaction was quenched by addition of 6 M HCl to a final pH of 4. The layers were separated and the organic layer was concentrated to a slush. Pentane was added and the product was isolated by filtration and dried to give the title compound (82.6 g, 80%).
後処理
- temperaturethe reaction mixture was heated up
- temperatureto reflux for 4 hours
- customThe reaction mixture was then carefully quenched into water
- customthe product was isolated by filtration
- additionAfter mixing for 1 h
- customthe reaction was quenched by addition of 6 M HCl to a final pH of 4
- customThe layers were separated
- concentrationthe organic layer was concentrated to a slush
- additionPentane was added
- customthe product was isolated by filtration
- customdried
出典と根拠
- ORDレコード
- ord-6ead266f18104284ab28669989c4738a
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07538105B2
関連ノート
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