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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → HCID 67512779、化合物

HRID 244375
ノート
印刷プレビュー

反応式

HRID 244375 の反応式
[OH:1][C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[C:4]([CH3:15])[CH:3]=1.[C:16](=O)([O-])[O-].[K+].[K+].O.C(O[CH2:27][CH3:28])(=O)C>CN(C)C=O.C1OCCOCCOCCOCCOCCOC1>[CH3:15][C:4]1[CH:3]=[C:2]([O:1][CH2:16][CH:27]=[CH2:28])[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]=1[C:6]([O:8][CH3:9])=[O:7]
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 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 58376048Methyl 4-hydroxy-2-methyl-5-nitrobenzoate

生成物 1

HCID 67512779HCID 67512779、化合物

試薬・触媒・溶媒 2

HCID 2855718-Crown-6触媒
HCID 6228
Dimethylformamide
溶媒

反応条件

温度
80 °C

実験手順

To a solution of methyl 4-hydroxy-2-methyl-5-nitrobenzoate (6.3 g) in N,N-dimethyl-formamide (150 ml) were added at room temperature 18-crown-6 (79 mg) and potassium carbonate (8.3 g), and the mixture was stirred at 80° C. for one hour. The mixture was cooled to room temperature, and to the reaction solution were added water and ethyl acetate, and the mixture was extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure to give the title compound (7.5 g).

後処理

  1. temperatureThe mixture was cooled to room temperature
  2. extractionthe mixture was extracted with ethyl acetate
  3. dry with materialThe organic layer was dried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-acb17f18e12e4257bed4406b09b9df21
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08658639B2

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