Ethyl bromoacetate → HCID 54158312、化合物
反応式
Br[CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].C(=O)([O-])[O-].[K+].[K+].[OH:14][C:15]1[CH:22]=[C:21]([CH3:23])[C:20]([CH3:24])=[CH:19][C:16]=1[CH:17]=[O:18]>CC(C)=O>[CH:17]([C:16]1[CH:19]=[C:20]([CH3:24])[C:21]([CH3:23])=[CH:22][C:15]=1[O:14][CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4])=[O:18]参加物
5
実験手順
0.808 ml of ethyl bromoacetate and 1 g of potassium carbonate were added to a solution of 838 mg of 2-hydroxy-4,5-dimethylbenzaldehyde (J.Chem.Soc. (1953) 820) in 150 ml of acetone. The suspension obtained was heated to reflux overnight and then filtered. The filtrate was concentrated. The crude product was isolated by extraction and purified by chromatography on silica gel and yielded 952 mg of ethyl (2-formyl-4,5-dimethyl-phenoxy)-acetate as a pale yellow solid.
後処理
- customThe suspension obtained
- temperaturewas heated
- temperatureto reflux overnight
- filtrationfiltered
- concentrationThe filtrate was concentrated
- customThe crude product was isolated by extraction
- custompurified by chromatography on silica gel
出典と根拠
- ORDレコード
- ord-ccede18c4da749e8bfc4bbeacd978ef2
- 出典データセット
- uspto-grants-2004_01
- 特許番号
- US06683215B2
反応ノート
読み込み中…