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Hydrochloric Acid → 6-(4-Ethoxycarbonylbutyl)oxycoumarin

HRID 1657049
ノート
印刷プレビュー

反応式

HRID 1657049 の反応式
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][C:7](=[O:12])[CH:6]=[CH:5]2.[H-].[Na+].Br[CH2:16][CH2:17][CH2:18][CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21].Cl>CN(C)C=O>[CH2:23]([O:22][C:20]([CH2:19][CH2:18][CH2:17][CH2:16][O:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][C:7](=[O:12])[CH:6]=[CH:5]2)=[O:21])[CH3:24]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 24758Sodium hydrideHCID 84580Ethyl 5-bromovalerateHCID 994776-hydroxy-2H-chromen-2-one

生成物 1

HCID 150296966-(4-Ethoxycarbonylbutyl)oxycoumarin

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
60 °C

実験手順

6-Hydroxycoumarin (405 mg; prepared in reference example 25) was dissolved in dry dimethylformamide (6 ml). Sodium hydride (60 mg) was added to the solution. The mixture was reacted for 15 min. Ethyl 5-bromopentanoate (0.48 ml) was added dropwise to the reaction solution. The mixture was stirred for 1 hr at 60° C. Ice-water was added to the reaction solution. The mixture was acidified with 1N hydrochloric acid. The mixture was extracted with ether. The extract was washed with water, dried anhydrous magnesium sulfate and then evaporated. The residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=4:1→2:1) to give the title compound (398 mg) having the following physical data.

後処理

  1. customThe mixture was reacted for 15 min
  2. extractionThe mixture was extracted with ether
  3. washThe extract was washed with water, dried anhydrous magnesium sulfate
  4. customevaporated
  5. customThe residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=4:1→2:1)

出典と根拠

ORDレコード
ord-caf32d2d81d94caab8d828b15217489d
出典データセット
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05256686

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート