反応式
Cl[C:2]1[C:7]([Cl:8])=[C:6](Cl)[C:5]([Cl:10])=[C:4]([C:11]([Cl:14])([Cl:13])[Cl:12])[N:3]=1.[CH3:15][OH:16].[CH3:17][O-:18].[Na+]>CS(C)=O>[Cl:8][C:7]1[C:2]([O:18][CH3:17])=[N:3][C:4]([C:11]([Cl:14])([Cl:13])[Cl:12])=[C:5]([Cl:10])[C:6]=1[O:16][CH3:15]参加物
実験手順
A 50.0 g portion (0.15 mol) of 2,3,4,5-tetrachloro-6-(trichloromethyl)pyridine was dissolved in 50 ml of warm dimethyl sulfoxide and 100 ml of methanol was added. Sodium methoxide (68.5 ml of 25 percent solution in methanol, 0.30 mol) was added, with stirring, over a 30 minute period and the resulting mixture was heated to reflux, with stirring, for two hours. After cooling, the mixture was poured into ice water and the aqueous mixture was extracted twice with methylene chloride. The extract was washed with water and evaporated to remove the methylene chloride. Traces of dimethyl sulfoxide remained. The residue was dissolved in ether and the ethereal solution was washed with water, dried over magnesium sulfate, and evaporated under reduced pressure to obtain 39.4 g of white solid product (81 percent of theory) melting at 67°-69° C. The proton nmr spectrum was consistent with the structure given.
後処理
- temperaturethe resulting mixture was heated
- temperatureto reflux
- stirringwith stirring, for two hours
- temperatureAfter cooling
- extractionthe aqueous mixture was extracted twice with methylene chloride
- washThe extract was washed with water
- customevaporated
- customto remove the methylene chloride
- dissolutionThe residue was dissolved in ether
- washthe ethereal solution was washed with water
- dry with materialdried over magnesium sulfate
- customevaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-fd1322b11ed8470093839001a6f2fbef
- 出典データセット
- uspto-grants-1988_01
- 特許番号
- US04717726
関連ノート
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