Thionyl Chloride → 3-(2-Chloroethyl)-1,4-dimethyl-2-piperazinone
反応式
S(Cl)([Cl:3])=O.O[CH2:6][CH2:7][CH:8]1[N:13]([CH3:14])[CH2:12][CH2:11][N:10]([CH3:15])[C:9]1=[O:16].C(=O)(O)[O-].[Na+]>C(Cl)Cl>[Cl:3][CH2:6][CH2:7][CH:8]1[N:13]([CH3:14])[CH2:12][CH2:11][N:10]([CH3:15])[C:9]1=[O:16]参加物
5
実験手順
Thionyl chloride (1.5 mL) was added dropwise to an ice cooled methylene chloride (5 mL) solution of 3-(2-hydroxyethyl)-1,4-dimethyl-2-piperazinone (0.40 g, described in Example 1). The reaction mixture was stirred for 30 min and poured on an ice solution of 10% sodium bicarbonate. The mixture was extracted with methylene chloride, and the organic extract was dried and evaporated to give the title compound: IR (CHCl3) 1635 cm-1 ; and NMR (CDCl3) δ 2.35 (s, 3H) and 2.90 (s, 3H).
後処理
- extractionThe mixture was extracted with methylene chloride
- extractionthe organic extract
- customwas dried
- customevaporated
出典と根拠
- ORDレコード
- ord-06f7e3a145ee4f469d08c31fbf695190
- 出典データセット
- uspto-grants-1985_05
- 特許番号
- US04515949
反応ノート
読み込み中…