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Ethyl bromoacetate → HCID 178472986、化合物

HRID 2225607
ノート
印刷プレビュー

反応式

HRID 2225607 の反応式
C(=O)([O-])[O-].[K+].[K+].[CH3:7][C@H:8]1[CH2:13][CH2:12][C@H:11]([NH:14][C:15](=[O:30])[CH:16]=[CH:17][C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[C:20]([O:26]C(=O)C)[CH:19]=2)[CH2:10][CH2:9]1.Br[CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34]>C(O)C>[CH3:7][C@H:8]1[CH2:13][CH2:12][C@H:11]([NH:14][C:15](=[O:30])[CH:16]=[CH:17][C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[C:20]([O:26][CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34])[CH:19]=2)[CH2:10][CH2:9]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 3

HCID 7748Ethyl bromoacetateHCID 11430Potassium CarbonateHCID 178490193HCID 178490193、化合物

生成物 1

HCID 178472986HCID 178472986、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

2.07 g of potassium carbonate was added to a solution of 4.97 g of N-(trans-4-methylcyclohexyl)-3-acetoxy-4-methoxycinnamamide (Example 193) in 200 ml of ethanol. The solution was stirred for 20 minutes, while it was refluxed. Next, 2.0 ml of ethyl bromoacetate was slowly added dropwise to the solution .by means of a dropping funnel. Thereafter, the solution was stirred for 2 hours. After reaction, the solution was allowed to cool to room temperature. The crystal and the potassium carbonate, both precipitated from the reaction solution, were filtered out, and the solvent was removed in vacuo from the filtrate. The product obtained was recrystallized from methylene chloride/ether, yielding 1.46 g of N-(trans-4-methylcyclohexyl)-3-(ethoxycarbonylmethoxy)-4-methoxycinnamamide (a compound the present invention) as white crystal, which had the following physiochemical properties:

後処理

  1. temperaturewas refluxed
  2. custommeans of a dropping funnel
  3. stirringThereafter, the solution was stirred for 2 hours
  4. customAfter reaction
  5. customThe crystal and the potassium carbonate, both precipitated from the reaction solution
  6. filtrationwere filtered out
  7. customthe solvent was removed in vacuo from the filtrate
  8. customThe product obtained
  9. customwas recrystallized from methylene chloride/ether

出典と根拠

ORDレコード
ord-ecd489bc601246e89af46ea256a0a811
出典データセット
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05344845

反応ノート

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