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Ammonium Chloride → Ethyl 2-azido-3-(5-methylthiophen-2-yl)acrylate

HRID 518123
ノート
印刷プレビュー

反応式

HRID 518123 の反応式
[N:1]([CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6])=[N+:2]=[N-:3].[O-]CC.[Na+].[CH3:14][C:15]1[S:19][C:18]([CH:20]=O)=[CH:17][CH:16]=1.[Cl-].[NH4+]>CO.O>[N:1]([C:4](=[CH:20][C:18]1[S:19][C:15]([CH3:14])=[CH:16][CH:17]=1)[C:5]([O:7][CH2:8][CH3:9])=[O:6])=[N+:2]=[N-:3]
参加物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 25517Ammonium ChlorideHCID 616635-Methyl-2-thiophenecarboxaldehydeHCID 69480Acetic acid, azido-, ethyl esterHCID 2723922Sodium ethoxide

生成物 1

HCID 76601917Ethyl 2-azido-3-(5-methylthiophen-2-yl)acrylate収率 72.1%

試薬・触媒・溶媒 2

HCID 887Methanol
溶媒
HCID 962Water溶媒

実験手順

To a solution of ethyl azidoacetate (10.6 g) in methanol (65 mL) was added sodium ethoxide (20% solution in ethanol, 27.2 g) under ice-cooling, and the mixture was stirred at the same temperature for 1 hour. 5-Methylthiophene-2-carbaldehyde (2.5 g) was added to this solution and the mixture was stirred at room temperature for 1 hour. To the reaction solution was added saturated ammonium chloride aqueous solution and water, and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=100/0−90/10) to give the title compound (3.39 g)

後処理

  1. temperaturecooling
  2. stirringthe mixture was stirred at room temperature for 1 hour
  3. extractionthe resulting mixture was extracted with ethyl acetate
  4. washThe organic layer was washed with brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=100/0−90/10)

出典と根拠

ORDレコード
ord-cc182f3ea8f94aaeb8e1da5b43927dd6
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09115144B2

反応ノート

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