Ethanol → HCID 21892028、化合物
反応式
C([CH:3]([C:7]([Cl:9])=O)C(Cl)=O)C.[Cl:10][C:11]1[C:12]([O:22][CH3:23])=[CH:13][CH:14]=[C:15]([CH:21]=1)[NH:16][C:17](=[O:20])[CH2:18]Cl.C(N(CC)CC)C.[CH2:31]([O-:33])[CH3:32].[Na+].[CH2:35]([OH:37])C>C(#N)C.O>[Cl:10][C:11]1[CH:21]=[C:15]2[C:14]([C:3]([CH2:7][Cl:9])=[C:18]([C:35]([O:33][CH2:31][CH3:32])=[O:37])[C:17](=[O:20])[NH:16]2)=[CH:13][C:12]=1[O:22][CH3:23]参加物
8
実験手順
A solution of ethylmalonyl chloride (17 ml, 131 mmol) is added dropwise under argon and at 0° C. to a solution of 5-chloro-2-chloroacetyl-4-methoxyaniline (17 g, 73 mmol) and triethylamine (18.5 ml, 131 mmol) in anhydrous acetonitrile (310 ml). Agitation is carried out for 2 hours at ambient temperature, then a solution of sodium ethanolate in ethanol (obtained by 1.88 g, 80 mmol, of sodium in 90 ml of ethanol) is added dropwise at 0° C. Agitation is carried out for 12 hours at ambient temperature. 300 ml of water is added, and agitation is again carried out for 20 minutes. The precipitate is filtered out; washed with water, with ethanol, and with ethyl ether. After drying under vacuum 16.7 g of a yellowish solid is obtained.
後処理
- waitAgitation is carried out for 12 hours at ambient temperature
- waitagitation is again carried out for 20 minutes
- filtrationThe precipitate is filtered out
- washwashed with water, with ethanol
- dry with materialAfter drying under vacuum 16.7 g of a yellowish solid
- customis obtained
出典と根拠
- ORDレコード
- ord-7be6534c8b5341dfaafc9d06fcb96636
- 出典データセット
- uspto-grants-2002_01
- 特許番号
- US06339091B1
反応ノート
読み込み中…