反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH2:8].[CH3:9][S:10][CH3:11].ClN1C(=O)CCC1=O.C(N(CC)CC)C>ClC(Cl)C.CCCCCC.CCOC(C)=O>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:9][S:10][CH3:11])[C:3]=1[NH2:8]参加物
実験手順
2-Chloro-phenylamine (12.76 g, 0.1 mole) and dimethyl sulfide (10 ml) were dissolved in dichloroethane (200 ml) and cooled in an ice-acetone-salt bath under a nitrogen atmosphere. N-chlorosuccinimide (14.70 g, 0.11 mole) dissolved in dichloroethane (300 ml) was slowly added via addition funnel over about 20-30 minutes. After stirring an hour beyond addition while allowing the reaction to reach room temperature, triethyl amine (30 ml) was added and the mixture was brought to reflux for 1 h and 20 minutes. The reaction was monitored by tlc (15:85 EtOAc:hexane on silica gel) which showed a single less polar product. The mixture was cooled and evaporated to dryness. The residue was taken up in methylene chloride, dry packed on silica gel, and placed onto a column of flash silica gel. The product was eluted from the column with 1:9 ethyl acetate:hexane to give 15.4 g of a homogeneous oil (82%), 2-chloro-6-methylsulfanylmethyl-phenylamine.
後処理
- temperaturecooled in an ice-acetone-salt bath under a nitrogen atmosphere
- additionwas slowly added via addition funnel over about 20-30 minutes
- customthe reaction
- customto reach room temperature
- temperatureto reflux for 1 h and 20 minutes
- temperatureThe mixture was cooled
- customevaporated to dryness
- customdry
- washThe product was eluted from the column with 1:9 ethyl acetate
出典と根拠
- ORDレコード
- ord-33e3ac922d8e4f8d978a1b211f1d4a44
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06852726B2
関連ノート
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