反応式
[OH:1][CH2:2][C:3]1[CH:8]=[N+:7]([O-:9])[C:6]([CH3:10])=[CH:5][N:4]=1.S(Cl)(Cl)=O.[Na].[CH:16]1C=CC=CC=1>CO.[Cl-].[Cl-].[Zn+2]>[CH3:16][O:1][CH2:2][C:3]1[CH:8]=[N+:7]([O-:9])[C:6]([CH3:10])=[CH:5][N:4]=1参加物
実験手順
2-Hydroxymethyl-5-methylpyrazine-4-oxide (3.5 g) was dissolved under stirring in a solution of 8 ml of thionyl chloride in 20 ml of dry benzene containing 0.5 g of ZnCl2, keeping the temperature below 30° C. The reaction mixture was cautiously warmed 3 hours at 60° C., then cooled to room temperature, and filtered. The solvent was evaporated under reduced pressure. The oily residue was dissolved in a solution of sodium methoxide in methyl alcohol, previously prepared dissolving 0.6 of sodium in 30 ml of methyl alcohol. After refluxing 4 hours, the reaction solution was cooled at room temperature, filtered and evaporated to dryness. The residue was taken up with water and repeatedly extracted with ethyl ether. The organic phase was washed with water, dried and the solvent was evaporated to dryness; the residue treated with pentane gave 2-methoxymethyl-5-methylpyrazine-4-oxide (1.5 g), m.p. 69°-72° C.
後処理
- customthe temperature below 30° C
- filtrationfiltered
- customThe solvent was evaporated under reduced pressure
- dissolutionThe oily residue was dissolved in a solution of sodium methoxide in methyl alcohol
- custompreviously prepared
- temperatureAfter refluxing 4 hours
- temperaturethe reaction solution was cooled at room temperature
- filtrationfiltered
- customevaporated to dryness
- extractionrepeatedly extracted with ethyl ether
- washThe organic phase was washed with water
- customdried
- customthe solvent was evaporated to dryness
- additionthe residue treated with pentane
出典と根拠
- ORDレコード
- ord-d46cfbf90a1146b6838aee08baba915f
- 出典データセット
- uspto-grants-1989_01
- 特許番号
- US04801711
関連ノート
読み込み中…