Water → HCID 14012477、化合物

HRID 568614ノート

反応式

HRID 568614 の反応式
Cl[C:2]1[C:16]([Cl:17])=[C:15]([OH:18])[CH:14]=[CH:13][C:3]=1[C:4](=[N:11][OH:12])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[H-].[Na+].Br[CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24].O>CN(C)C=O.C1(C)C=CC=CC=1>[CH2:26]([O:25][C:23](=[O:24])[CH2:22][O:18][C:15]1[CH:14]=[CH:13][C:3]2[C:4]([C:5]3[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=3)=[N:11][O:12][C:2]=2[C:16]=1[Cl:17])[CH3:27]

参加物

7

反応物 4

HCID 962WaterHCID 7748Ethyl bromoacetateHCID 24758Sodium hydride2 回HCID 136393678HCID 136393678、化合物

生成物 1

HCID 14012477HCID 14012477、化合物

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒HCID 6228Dimethylformamide溶媒2 回

実験手順

A solution of 2,3-dichloro-4-hydroxybenzophenone oxime and 2.6 g of sodium hydride in 50 ml of dimethylformamide and 50 ml of toluene is heated to 118° C. and maintained at this temperature for 50 minutes. Thereafter, the reaction is permitted to cool prior to the dropwise addition of 7.9 g of ethyl bromoacetate in 50 ml of dimethylformamide. After the addition is complete the reaction mixture is stirred at ambient temperature for 40 minutes. To the well stirred mixture water is added dropwise to decompose any excess sodium hydride. The toluene is evaporated under vacuum and the resulting precipitate is collected by filtration and then rinsed with ether to yield the product ethyl[(7-chloro-3-phenyl-1,2-benzisoxazol-6-yl)oxy]acetate having a melting point of 130° to 132° C.

後処理

  1. temperaturemaintained at this temperature for 50 minutes
  2. temperatureto cool
  3. additionAfter the addition
  4. additionis added dropwise
  5. customThe toluene is evaporated under vacuum
  6. filtrationthe resulting precipitate is collected by filtration
  7. washrinsed with ether

出典と根拠

ORDレコード
ord-6fd268a9c34d45ee8782c940b997e608
出典データセット
uspto-grants-1988_03
特許番号
US04728662

反応ノート

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