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Sodium Hydroxide → HCID 23083190、化合物

HRID 2422294
ノート
印刷プレビュー

反応式

HRID 2422294 の反応式
[CH3:1][C:2]1[CH:28]=[CH:27][CH:26]=[C:25]([CH3:29])[C:3]=1[O:4][C:5]1[CH:6]=[C:7]([CH:22]=[CH:23][CH:24]=1)[CH2:8][O:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][CH2:17][C:18]([O:20]C)=[O:19])=[CH:12][CH:11]=1.[OH-].[Na+]>CO>[CH3:1][C:2]1[CH:28]=[CH:27][CH:26]=[C:25]([CH3:29])[C:3]=1[O:4][C:5]1[CH:6]=[C:7]([CH:22]=[CH:23][CH:24]=1)[CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]([CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[CH:14][CH:15]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 23083008HCID 23083008、化合物

生成物 1

HCID 23083190HCID 23083190、化合物収率 64.3%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution (5.0 mL) of methyl 3-(4-((3-(2,6-dimethylphenoxy)benzyl)oxy)phenyl)propanoate (0.24 g, 0.62 mmol) in methanol was added 1N aqueous sodium hydroxide solution (1.2 mL), and the mixture was stirred at room temperature for 2 hrs. The reaction mixture was concentrated, and the residue was diluted with ethyl acetate, washed with 1N hydrochloric acid and water, dried, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=3/2-1/4) to give the title compound (0.15 g, yield 64%) as colorless crystals.

後処理

  1. concentrationThe reaction mixture was concentrated
  2. additionthe residue was diluted with ethyl acetate
  3. washwashed with 1N hydrochloric acid and water
  4. customdried
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate=3/2-1/4)

出典と根拠

ORDレコード
ord-c3f89e9b805a4f6796a41c7988548aa8
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07960369B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート