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Water → 3(E)-[4-Ethoxy-3-Propoxyphenyl]Acrylic Acid

HRID 987873
ノート
印刷プレビュー

反応式

HRID 987873 の反応式
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7](/[CH:10]=[CH:11]/[C:12]([O:14]C)=[O:13])=[CH:6][C:5]=1[O:16][CH2:17][CH2:18][CH3:19])[CH3:2].[OH-].[K+].O>CO>[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7](/[CH:10]=[CH:11]/[C:12]([OH:14])=[O:13])=[CH:6][C:5]=1[O:16][CH2:17][CH2:18][CH3:19])[CH3:2]
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

5

反応物 3

HCID 962WaterHCID 14797Potassium HydroxideHCID 22987083methyl 3(E)-[4-ethoxy-3-propoxyphenyl]acrylate

生成物 1

HCID 177755763(E)-[4-Ethoxy-3-Propoxyphenyl]Acrylic Acid

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
70 °C

実験手順

1.0 g (3.78 mmol) of methyl 3(E)-[4-ethoxy-3-propoxyphenyl]acrylate are suspended in 50 ml of a 10% solution of potassium hydroxide in methanol. 2 ml of water are then added and the mixture is heated to 70° C. for 3 hours and then cooled. Thereafter, the reaction mixture is partitioned between diethyl ether and water, the organic phase is washed several times with saturated sodium chloride solution and the combined aqueous phases are adjusted to pH 4 with a 25% hydrochloric acid solution and extracted several times with methylene chloride. The methylene chloride phases are then combined, dried over magnesium sulfate, filtered and evaporated down. This gives 3(E)-[4-ethoxy-3-propoxyphenyl]acrylic acid.

後処理

  1. temperaturecooled
  2. customThereafter, the reaction mixture is partitioned between diethyl ether and water
  3. washthe organic phase is washed several times with saturated sodium chloride solution
  4. extractionextracted several times with methylene chloride
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. customevaporated down

出典と根拠

ORDレコード
ord-8ca57a9e31f24c40a0e88ed4be42db70
出典データセット
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06632909B2

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