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Water → 2-[4-(2-Oxopyrrolidin-1-yl)phenyl]acetic acid

HRID 1373239
ノート
印刷プレビュー

反応式

HRID 1373239 の反応式
[OH-].[Na+].C([O:5][C:6](=[O:20])[CH2:7][C:8]1[CH:13]=[CH:12][C:11]([N:14]2[CH2:18][CH2:17][CH2:16][C:15]2=[O:19])=[CH:10][CH:9]=1)C.O.S([O-])(O)(=O)=O.[K+]>O1CCCC1.C(O)C>[O:19]=[C:15]1[CH2:16][CH2:17][CH2:18][N:14]1[C:11]1[CH:12]=[CH:13][C:8]([CH2:7][C:6]([OH:20])=[O:5])=[CH:9][CH:10]=1
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

7

反応物 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 516920Potassium bisulfateHCID 21072938HCID 21072938、化合物

生成物 1

HCID 71307492-[4-(2-Oxopyrrolidin-1-yl)phenyl]acetic acid収率 58.5%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒
HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
60 °C

実験手順

Aqueous 1 N sodium hydroxide solution (10 ml, 10 mmols) was added to a solution of ethyl[4-(2-oxopyrrolidin-1-yl)phenyl]acetate (0.97 g, 3.9 mmols) in tetrahydrofuran (20 ml) and ethanol (20 ml). The resulting mixture was stirred at 60° C. for 1 hour. Water was added to the reaction mixture, which was acidified with potassium hydrogensulfate added thereto, and then extracted with ethyl acetate. The extract was washed with water, and then dried with anhydrous magnesium sulfate. This was concentrated under reduced pressure, and the residue was crystallized from hexane/ethanol to give a solid of [4-(2-oxopyrrolidin-1-yl)phenyl]acetic acid (0.5 g, 57%).

後処理

  1. additionadded
  2. extractionextracted with ethyl acetate
  3. washThe extract was washed with water
  4. dry with materialdried with anhydrous magnesium sulfate
  5. concentrationThis was concentrated under reduced pressure
  6. customthe residue was crystallized from hexane/ethanol

出典と根拠

ORDレコード
ord-1012e025c6884ec3a73c2cb36bcaf490
出典データセット
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07160887B1

反応ノート

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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