反応式
[NH2:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[OH:8].[Cl:9][CH2:10][C:11](Cl)=[O:12]>>[Cl:9][CH2:10][C:11]([NH:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[OH:8])=[O:12]参加物
3
実験手順
A solution of 4-amino-3-hydroxypyridine (7 g, 0.06 mol) and chloroacetyl chloride (50 ml) was refluxed for 2 hours, cooled and the excess solvent was removed by vacuum distillation. The crude material was dissolved in water, neutralized with Na2CO3 and the solid precipitated filtered and air dried to give the desired product, m.p. 155°-158° C. The structural assignment was supported by the proton NMR spectrum.
後処理
- temperaturecooled
- customthe excess solvent was removed by vacuum distillation
- dissolutionThe crude material was dissolved in water
- customthe solid precipitated
- filtrationfiltered
- customair dried
出典と根拠
- ORDレコード
- ord-0e717692545847bf99de662dd998060e
- 出典データセット
- uspto-grants-1997_07
- 特許番号
- US05652363
関連ノート
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