Acetic Acid → HCID 178456787、化合物
反応式
[H-].[Na+].[C:3]([CH:5]([CH3:13])[C:6](OC(C)(C)C)=O)#[N:4].Cl[C:15]1[N:16]=[N:17]C(Cl)=[CH:19][CH:20]=1.C(O)(=[O:24])C>O1CCCC1>[OH:24][C:15]1[N:16]=[N:17][C:6]([CH:5]([CH3:13])[C:3]#[N:4])=[CH:19][CH:20]=1参加物
実験手順
60.4 g (2.02 mol) of 80% strength sodium hydride in white oil are suspended in 2 liters of tetrahydrofuran and 311.8 g (2.02 mol) of tert.-butyl 2-cyanopropionate are added dropwise at 20°-30° C. During the course of 45 minutes this clear solution is added dropwise to a solution of 298 g (2.0 mol) of 3,6-dichloropyridazine and the mixture is heated under reflux for 2 hours. 317 ml of acetic acid are then added and the solvent is removed in vacuo. The residue is taken up in a mixture of 6,400 ml of acetic acid, 250 ml of acetic anhydride and 32 g of p-toluenesulfonic acid monohydrate, heated under reflux for 3 hours and again brought to dryness in vacuo. The residue is suspended in a little water, adjusted to pH 5 with sodium hydroxide solution and the water removed by evaporation. The residue is extracted hot using ethyl acetate. 99.7 g (33% of theory) of crude product are thus obtained, which can be employed for the following reaction without further processing.
後処理
- temperaturethe mixture is heated
- temperatureunder reflux for 2 hours
- customthe solvent is removed in vacuo
- additionThe residue is taken up in a mixture of 6,400 ml of acetic acid, 250 ml of acetic anhydride and 32 g of p-toluenesulfonic acid monohydrate
- temperatureheated
- temperatureunder reflux for 3 hours
- customthe water removed by evaporation
- extractionThe residue is extracted hot
- custom99.7 g (33% of theory) of crude product are thus obtained
- customwhich can be employed for the following reaction without further processing
出典と根拠
- ORDレコード
- ord-f796673195304f088d5b5eb889344b33
- 出典データセット
- uspto-grants-1990_10
- 特許番号
- US04966902
反応ノート
読み込み中…