N-bromobutanimide → Ethyl 2-(bromomethyl)thiazole-5-carboxylate
反応式
[CH2:1]([O:3][C:4]([C:6]1[S:10][C:9]([CH3:11])=[N:8][CH:7]=1)=[O:5])[CH3:2].[Br:12]N1C(=O)CCC1=O>C(OCC)(=O)C>[Br:12][CH2:11][C:9]1[S:10][C:6]([C:4]([O:3][CH2:1][CH3:2])=[O:5])=[CH:7][N:8]=1参加物
4
実験手順
2-Methyl-5-thiazolecarboxylic acid ethyl ester (3.9 g) (J. Am. Chem. Soc. 1982, 104, 4461), N-bromosuccinimide (4.1 g) and catalytic azoisobutyronitrile in ethyl acetate (150 ml) was heated at reflux and under a 500 W halogen lamp for 16 hours. The solution was washed with water, dried (MgSO4) and evaporated. Purification was by chromatography eluting with 50% ethyl acetate in isohexane. Yield 1.5 g.
後処理
- washThe solution was washed with water
- dry with materialdried (MgSO4)
- customevaporated
- customPurification
- washeluting with 50% ethyl acetate in isohexane
出典と根拠
- ORDレコード
- ord-a7c83e01a09e42c2a564b80d2b2979fd
- 出典データセット
- uspto-grants-2000_12
- 特許番号
- US06162808
反応ノート
読み込み中…