Iodoethane → Methyl 2-(p-chlorophenoxy)-2-[p-(p-chlorophenoxy)phenyl]butyrate
反応式
[Cl:1][C:2]1[CH:28]=[CH:27][C:5]([O:6][C:7]([C:13]2[CH:18]=[CH:17][C:16]([O:19][C:20]3[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=3)=[CH:15][CH:14]=2)([CH3:12])[C:8]([O:10][CH3:11])=[O:9])=[CH:4][CH:3]=1.Cl[C:30]1C=CC(OC(C2C=CC(OC3C=CC(Cl)=CC=3)=CC=2)C(OC)=O)=CC=1.CN(C)P(N(C)C)(N(C)C)=O.C(I)C>O1CCCC1.O>[Cl:1][C:2]1[CH:28]=[CH:27][C:5]([O:6][C:7]([C:13]2[CH:18]=[CH:17][C:16]([O:19][C:20]3[CH:21]=[CH:22][C:23]([Cl:26])=[CH:24][CH:25]=3)=[CH:15][CH:14]=2)([CH2:12][CH3:30])[C:8]([O:10][CH3:11])=[O:9])=[CH:4][CH:3]=1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
A solution of 0.015 mole of lithium N,N-diisopropylamide (prepared as in example 55) in tetrahydrofuran is chilled to -65° C to -75° C. To the solution is added methyl (p-chlorophenoxy)[p-(p-chlorophenoxy)phenyl]acetate in 10 ml of tetrahydrofuran. To the mixture is added 5 ml of hexamethylphosphoramide and while chilling to -65° C to -75° C, 4.68 g of ethyl iodide is added. After 1 hr., the mixture is allowed to warm to room temperature and stir overnight. The mixture is poured into water and extracted with ether. The ether extracts are washed with 10% hydrochloric acid, water, saturated NaHCo3, saturated NaCl solution and dried (MgSO4). Evaporation of the solvent gives the product as an oil.
後処理
- temperaturewhile chilling to -65° C to -75° C
- extractionextracted with ether
- washThe ether extracts are washed with 10% hydrochloric acid, water, saturated NaHCo3, saturated NaCl solution
- dry with materialdried (MgSO4)
- customEvaporation of the solvent
出典と根拠
- ORDレコード
- ord-17865f9a5ccf4750a205b5d164d67371
- 出典データセット
- uspto-grants-1978_11
- 特許番号
- US04125729
反応ノート
読み込み中…