Ethyl bromoacetate → Ethyl[(6,7-dichlorobenzo[b]thien-5-yl)oxy]acetate

HRID 485849

反応式

HRID 485849 の反応式
[Cl:1][C:2]1[C:3]([OH:12])=[CH:4][C:5]2[CH:9]=[CH:8][S:7][C:6]=2[C:10]=1[Cl:11].Br[CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[Cl:1][C:2]1[C:3]([O:12][CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:4][C:5]2[CH:9]=[CH:8][S:7][C:6]=2[C:10]=1[Cl:11]

参加物

5

反応物 3

HCID 7748Ethyl bromoacetateHCID 11430Potassium CarbonateHCID 132899976,7-Dichloro-1-benzothiophene-5-ol

生成物 1

HCID 13289999Ethyl[(6,7-dichlorobenzo[b]thien-5-yl)oxy]acetate収率 63.8%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A mixture of 3.6 g of 6,7-dichloro-5-hydroxybenzo[b]thiophene, 3.0 g of ethyl bromoacetate, 1.5 g of potassium carbonate and 40 ml of anhydrous dimethylformamide is stirred at 70°-80° for 16 hours. The cooled mixture is diluted with ice-water (200 g) and the solid collected by filtration. Recrystallization of the crude product from acetone-hexane gives 3.2 g of ethyl [(6,7-dichlorobenzo[b]thien-5-yl)oxy]acetate as yellowish needles, mp 92°-93°.

後処理

  1. filtrationthe solid collected by filtration
  2. customRecrystallization of the crude product from acetone-hexane

出典と根拠

ORDレコード
ord-1930dce74430403d89f3c7b8d41e4795
出典データセット
uspto-grants-1985_08
特許番号
US04537976

関連ノート

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