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Potassium Hydroxide → (4-Pyridin-2-YL-phenyl)-acetic acid

HRID 2213529
ノート
印刷プレビュー

反応式

HRID 2213529 の反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][C:14]([O:16]C)=[O:15])=[CH:9][CH:8]=1.[OH-].[K+]>O1CCCC1.O>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][C:14]([OH:16])=[O:15])=[CH:9][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 14797Potassium HydroxideHCID 12094242Methyl 2-(4-(pyridin-2-yl)phenyl)acetate

生成物 1

HCID 504301(4-Pyridin-2-YL-phenyl)-acetic acid

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

700 mg (3.11 mol) of methyl [4-(2-pyridinyl)phenyl]acetate are initially charged in 5 ml of tetrahydrofuran and, at room temperature, admixed with 6.2 ml of a 1M potassium hydroxide solution in water. The mixture is then stirred at room temperature for 18 h, most of the solvent is removed under reduced pressure and the residue is taken up in 10 ml of water and adjusted to a pH of about 5 using 2N hydrochloric acid. The aqueous phase was extracted twice, in each case with 10 ml of dichloromethane, the combined organic phases were dried over magnesium sulphate and the solvent was removed under reduced pressure, giving the compound of Example VIII in the form of a solid.

後処理

  1. customis removed under reduced pressure
  2. extractionThe aqueous phase was extracted twice, in each case with 10 ml of dichloromethane
  3. dry with materialthe combined organic phases were dried over magnesium sulphate
  4. customthe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-23fd563ab03e40bdbdddc196e35192e5
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07105553B2

反応ノート

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