反応式
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[O:11][CH3:12].[OH-].[Na+].[Cl:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][C:23]#[N:24])=[CH:18][CH:17]=1.Cl>[Cl-].C([N+](CC)(CC)CC1C=CC=CC=1)C.O1CCCC1>[Cl:15][C:16]1[CH:21]=[CH:20][C:19]([CH:22]([C:2]2[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=2[O:11][CH3:12])[C:23]#[N:24])=[CH:18][CH:17]=1参加物
実験手順
To a stirred mixture of 68 parts of 1-chloro-2-methoxy-4-nitrobenzene, 230 parts of a sodium hydroxide solution 50%, 5 parts of N,N,N-triethylbenzenemethanaminium chloride and 360 parts of tetrahydrofuran is added dropwise, during a 5 minutes period, a solution of 43.2 parts of 4-chlorobenzeneacetonitrile in 90 parts of tetrahydrofuran. Upon completion, stirring is continued for 4 hours at 60° C. The reaction mixture is poured into 2000 parts of crushed ice. The whole is acidified with concentrated hydrochloric acid. The layers are separated. The aqueous phase is extracted with dichloromethane. The combined extracts are dried, filtered and evaporated. The residue is crystallized from 2,2'-oxybispropane. The product is filtered off and dried, yielding α-(4-chlorophenyl)-2-methoxy-4-nitrobenzeneacetonitrile.
後処理
- additionis added dropwise, during a 5 minutes period
- additionThe reaction mixture is poured into 2000 parts of crushed ice
- customThe layers are separated
- extractionThe aqueous phase is extracted with dichloromethane
- customThe combined extracts are dried
- filtrationfiltered
- customevaporated
- customThe residue is crystallized from 2,2'-oxybispropane
- filtrationThe product is filtered off
- customdried
出典と根拠
- ORDレコード
- ord-fff9ae469d1a457387a4a6f72779f1b8
- 出典データセット
- uspto-grants-1988_08
- 特許番号
- US04767760
関連ノート
読み込み中…