Iodoethane → Methyl 2-(5-indanyloxy)-2-[p-(p-chlorophenoxy)phenyl]butyrate
反応式
Cl[C:2]1C=CC(OC(C2C=CC(OC3C=CC(Cl)=CC=3)=CC=2)(C)C(OC)=O)=C[CH:3]=1.[CH2:29]1[C:37]2[C:32](=[CH:33][C:34]([O:38][CH:39]([C:44]3[CH:49]=[CH:48][C:47]([O:50][C:51]4[CH:56]=[CH:55][C:54]([Cl:57])=[CH:53][CH:52]=4)=[CH:46][CH:45]=3)[C:40]([O:42][CH3:43])=[O:41])=[CH:35][CH:36]=2)[CH2:31][CH2:30]1.CN(C)P(N(C)C)(N(C)C)=O.C(I)C>O1CCCC1.O>[CH2:29]1[C:37]2[C:32](=[CH:33][C:34]([O:38][C:39]([C:44]3[CH:49]=[CH:48][C:47]([O:50][C:51]4[CH:56]=[CH:55][C:54]([Cl:57])=[CH:53][CH:52]=4)=[CH:46][CH:45]=3)([CH2:2][CH3:3])[C:40]([O:42][CH3:43])=[O:41])=[CH:35][CH:36]=2)[CH2:31][CH2:30]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 (5-indanyloxy)[p-(p-chlorophenoxy)phenyl]acetate in tetrahydrofuran. To the mixture is added 4 ml of hexamethylphosphoramide and while chilling to -65° C. to -75° C., 4.68 g of ethyl iodide is added. After 2 hr., the mixture is allowed to warm to room temperature and stirr 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-20ae915ded0e42028ed5d26a6feb48a5
- 出典データセット
- uspto-grants-1979_09
- 特許番号
- US04168385
反応ノート
読み込み中…