ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
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
  1. ホーム
  2. /反応

Hydrochloric Acid → HCID 23508318、化合物

HRID 1883713
ノート
印刷プレビュー

反応式

HRID 1883713 の反応式
C([NH:4][C:5]1[CH:6]=[CH:7][C:8]([CH:14]([CH3:21])[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[C:9]2[C:13]=1[CH2:12][CH2:11][CH2:10]2)(=O)C.[ClH:22]>>[ClH:22].[NH2:4][C:5]1[CH:6]=[CH:7][C:8]([CH:14]([CH3:21])[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[C:9]2[C:13]=1[CH2:12][CH2:11][CH2:10]2
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

3

反応物 2

HCID 313Hydrochloric AcidHCID 23508311HCID 23508311、化合物

生成物 1

HCID 23508318HCID 23508318、化合物

反応条件

温度
118 °C

実験手順

Ethyl 3-[7-acetylamino-indan-4-yl]-butanoate (1.66 g, Reference Example 6) was treated with 6M aqueous hydrochloric acid. The stirred mixture was heated at 118° C. for 4 hours, then left to stand at room temperature for 48 hours and then evaporated. The residue was treated with ethanol (100 mL) and concentrated hydrochloric acid (4 drops). This mixture was heated at reflux for 2.5 hours, then allowed to stand at room temperature for 16 hours and then evaporated. The residue was dissolved in a little ethanol and the solution was evaporated. The residue was dried under high vacuum to give the title compound (1.57 g) as a fine solid.

後処理

  1. waitleft
  2. custom
evaporated
  • additionThe residue was treated with ethanol (100 mL) and concentrated hydrochloric acid (4 drops)
  • temperatureThis mixture was heated
  • temperatureat reflux for 2.5 hours
  • waitto stand at room temperature for 16 hours
  • customevaporated
  • dissolutionThe residue was dissolved in a little ethanol
  • customthe solution was evaporated
  • customThe residue was dried under high vacuum
  • 出典と根拠

    ORDレコード
    ord-e306141cc85b4f0ab9bdf8e54c7f6d9e
    出典データセット
    uspto-grants-2004_07
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06762199B2

    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